Competency Map: Physician | Genetics/Genomics Resources

1: FAMILY HISTORY
- P-FH1A: Patient Care
  - 1A1: Conduct patient interview to assemble family history
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - GeneReviews
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetic Medicine and Primary Care Infographic
    - Genetics in Primary Care Institute Video Testimonials
    - Genetics in Primary Care Institute Family History Tools
    - Coding Fact Sheet for Genetics in Primary Care
    - Genetics in Primary Care Institute Webinar Series
    - Hereditary colorectal cancers
    - Primary Care and Genetics and Genomics
    - Family History in Primary Care Pediatrics
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - GEC KO
  - 1A2: Use standard pedigree symbols in assembling family history
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - GeneReviews
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Genetics in Primary Care
    - Genetics in Primary Care Institute Webinar Series
    - Primary Care and Genetics and Genomics
    - Family History in Primary Care Pediatrics
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - GEC KO
  - 1A4: Use empirical risk figures to provide appropriate information for complex (multifactorial) medical conditions.
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - GeneReviews
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetics in Primary Care Institute Family History Tools
    - Primary Care and Genetics and Genomics
    - Family History in Primary Care Pediatrics
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - GEC KO
  - 1A5: Recognize that traits may cluster in families due to multifactorial rather than Mendelian patterns of inheritance
    - NHGRI Genomics in Medicine Lecture Series
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - PDQ Cancer Information Summaries: Genetics
    - GeneReviews
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Genetics in Primary Care
    - Genetic testing for hereditary breast cancer
    - Primary Care and Genetics and Genomics
    - Family History in Primary Care Pediatrics
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - GEC KO
  - 1A6: Formulate an action plan to address relevant family history information
    - National Genetics and Genomics Education Centre (UK)
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - PDQ Cancer Information Summaries: Genetics
    - GeneReviews
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Genetics in Primary Care
    - Genetics in Primary Care Institute Family History Tools
    - Primary Care and Genetics and Genomics
    - Family History in Primary Care Pediatrics
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
- P-FH1B: Knowledge for Practice
  - 1B1: Describe the basic patterns of Mendelian inheritance
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - GeneReviews
    - Genetics Home Reference
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American College of Obstetricians and Gynecologists WEBTREATS: Genetics, Genomics, and the Human Genome Project
    - Family History in Primary Care Pediatrics
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - Coursera Course: Genomic and Precision Medicine
    - Family History in Cancer Risk Assessment, Testing and Management
  - 1B2: Explain the difference between Mendelian and multifactorial inheritance
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - GeneReviews
    - Genetics Home Reference
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American College of Obstetricians and Gynecologists WEBTREATS: Genetics, Genomics, and the Human Genome Project
    - Family History in Primary Care Pediatrics
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - Coursera Course: Genomic and Precision Medicine
    - Family History in Cancer Risk Assessment, Testing and Management
- P-FH1C: Practice-Based Learning and Improvement
  - 1C1: Incorporate family history information into health record
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Genetics in Primary Care
    - National Cancer Institute Cancer Risk Prediction and Assessment: Bibliography of Risk Prediction Models
    - National Coalition for Health Professional Education (NCHPEG)
- P-FH1D: Interpersonal and Communication Skills
  - 1D1: Explain and document findings from family history to patient, including implications for other family members
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - GeneReviews
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Genetics in Primary Care
    - Genetic Medicine and Primary Care Infographic
    - How to Build a Genetic Patient Registry
    - Family History in Primary Care Pediatrics
    - National Coalition for Health Professional Education (NCHPEG)
    - GEC KO
    - Family History in Cancer Risk Assessment, Testing and Management
- P-FH1E: Professionalism
  - 1E1: Respect privacy of patient and family members in assembling and documenting family history
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - Primary Care and Genetics and Genomics
    - Family History in Primary Care Pediatrics
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
    - GEC KO
  - 1E2: Explain to patient relevant social and legal risks related to family history as well as relevant legal protections
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetic Medicine and Primary Care Infographic
    - Genetics in Primary Care Institute Family History Tools
    - Genetics in Primary Care Institute Webinar Series
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - Genetic testing for hereditary breast cancer
    - Primary Care and Genetics and Genomics
    - Family History in Primary Care Pediatrics
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
    - ASCO Cancer Genetics Program
    - GEC KO
    - Family History in Cancer Risk Assessment, Testing and Management
  - 1E3: Recognize the potential of family history information to reveal unexpected family relationships such as consanguinity or misattributed paternity
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - GeneReviews
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - Primary Care and Genetics and Genomics
    - Family History in Primary Care Pediatrics
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
    - ASCO Cancer Genetics Program
    - GEC KO
- P-FH1F: Systems-Based Practice
  - 1F1: Focus family history on problems relevant to the individual patient’s health
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - PediaGene Smartphone / Tablet App
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - Coding Fact Sheet for Genetics in Primary Care
    - Hereditary colorectal cancers
    - Colorectal Cancer
    - National Coalition for Health Professional Education (NCHPEG)
    - Family History in Cancer Risk Assessment, Testing and Management
  - 1F2: Facilitate patient’s desire to communicate relevant family history information among health providers and family members
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - PediaGene Smartphone / Tablet App
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - National Coalition for Health Professional Education (NCHPEG)
    - Family History in Cancer Risk Assessment, Testing and Management
- P-FH1G: Interprofessional Collaboration
  - 1G1: Make appropriate referrals for specialty evaluation based on results of family history
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - PDQ Cancer Information Summaries: Genetics
    - GeneReviews
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetic Medicine and Primary Care Infographic
    - Genetics in Primary Care Institute Webinar Series
    - Genetic Counseling
    - Family History in Primary Care Pediatrics
    - National Coalition for Health Professional Education (NCHPEG)
    - GEC KO
    - Family History in Cancer Risk Assessment, Testing and Management
- P-FH1H: Personal and Professional Development
  - 1H1: Identify sources of information on genetic disorders, such as OMIM (online Mendelian Inheritance in Man) and GeneReviews
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - Genetics in Primary Care
    - Genetics in Primary Care Institute Webinar Series
    - Hereditary pancreatitis
    - Hereditary colorectal cancers
    - Primary Care and Genetics and Genomics
    - National Cancer Institute Cancer Risk Prediction and Assessment: Bibliography of Risk Prediction Models
    - Genetics
    - Orphanet
    - GEC KO
    - Family History in Cancer Risk Assessment, Testing and Management
  - 1H2: Maintain continuing medical education on matters of medical genetics
    - NHGRI Genomics in Medicine Lecture Series
    - OMIM
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - Genetics in Primary Care Institute Webinar Series
    - Primary Care and Genetics and Genomics
    - National Cancer Institute Understanding Cancer Series
    - Genetics
    - Coursera Course: Genomic and Precision Medicine
    - GEC KO
    - Family History in Cancer Risk Assessment, Testing and Management
2: GENOMIC TESTING
- P-GT2A: Patient Care
  - 2A1: Discuss the indications for genomic testing – specifically the benefits, risks, and alternatives
    - NHGRI Genomics in Medicine Lecture Series
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Genetic Testing Registry
    - GeneReviews
    - Genetics Home Reference
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Introduction to the Newborn Screening Fact Sheets
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetic Medicine and Primary Care Infographic
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - Genetics in Primary Care Institute Video Testimonials
    - American College of Obstetricians and Gynecologists Committee Opinion: Personalized Genomic Testing for Disease Risk
    - Genetics in Primary Care Institute Webinar Series
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - DNA from A to Z & Back Again
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Hereditary colorectal cancers
    - Primary Care and Genetics and Genomics
    - Breast Cancer Clinical Recommendations
    - Cardiovascular disease
    - Colorectal Cancer
    - National Cancer Institute Understanding Cancer Series
    - Venous Thromboembolism
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
    - Recommendations of the American Academy of Ophthalmology Task Force on Genetic Testing
    - GEC KO
    - Family History in Cancer Risk Assessment, Testing and Management
  - 2A2: Explain the implications of placing genomic test results in the patient’s medical record
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - GeneReviews
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - National Cancer Institute Understanding Cancer Series
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - GEC KO
  - 2A3: Discuss the possibility of incidental findings and how they will be handled
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - National Cancer Institute Understanding Cancer Series
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
  - 2A4: Discuss risks of having genomic testing done: e.g., psychological implications for the individual as well as the family; the potential for discrimination; and the potential effect on insurance coverage.
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - GeneReviews
    - Genetics Home Reference
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Introduction to the Newborn Screening Fact Sheets
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American College of Obstetricians and Gynecologists Committee Opinion: Personalized Genomic Testing for Disease Risk
    - Genetics in Primary Care Institute Webinar Series
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - National Cancer Institute Understanding Cancer Series
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - GEC KO
  - 2A5: Explain to the patient issues of costs and financial coverage of genomic testing
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - GeneReviews
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Genetics in Primary Care Institute Video Testimonials
    - Coding Fact Sheet for Genetics in Primary Care
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - Genetic Testing Reimbursement and Regulation…What You Need to Know
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
  - 2A6: Order, interpret, and communicate the results of appropriate genomic tests, within the physician’s scope of practice
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - GeneReviews
    - Genetics Home Reference
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Introduction to the Newborn Screening Fact Sheets
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetic Medicine and Primary Care Infographic
    - Genetics in Primary Care Institute Webinar Series
    - Massively parallel (Next-generation) sequencing primer
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - DNA sequence nomenclature and variant interpretation
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Hereditary colorectal cancers
    - Primary Care and Genetics and Genomics
    - Cardiovascular disease
    - National Cancer Institute Understanding Cancer Series
    - Venous Thromboembolism
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - GEC KO
  - 2A7: Provide referral to an appropriate specialist for genomic testing of a condition outside the physician’s scope of practice
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Genetic Testing Registry
    - GeneReviews
    - Genetics Home Reference
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetic Medicine and Primary Care Infographic
    - Genetics in Primary Care Institute Family History Tools
    - American College of Obstetricians and Gynecologists Committee Opinion: Personalized Genomic Testing for Disease Risk
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - Breast Cancer Clinical Recommendations
    - National Cancer Institute Understanding Cancer Series
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - Recommendations of the American Academy of Ophthalmology Task Force on Genetic Testing
    - GEC KO
    - Family History in Cancer Risk Assessment, Testing and Management
  - 2A8: Respond to the results of an abnormal genetic screening test, such as newborn screening, including immediate management and appropriate referral
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Genetic Testing Registry
    - GeneReviews
    - Genetics Home Reference
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetics in Primary Care Institute Video Testimonials
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - Breast Cancer Clinical Recommendations
    - Genetics
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - Recommendations of the American Academy of Ophthalmology Task Force on Genetic Testing
    - GEC KO
- P-GT2B: Knowledge for Practice
  - 2B1: Describe the major forms of genomic variability
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - American College of Obstetricians and Gynecologists WEBTREATS: Genetics, Genomics, and the Human Genome Project
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - CAP’s Genomic Analysis Resource Guide
    - Coursera Course: Genomic and Precision Medicine
    - Training Residents in Genomics (TRIG) Working Group Genomic Pathology Workshop Handbook and Toolkit
  - 2B2: Explain how different genomic changes may result in different phenotypes
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - CAP’s Genomic Analysis Resource Guide
    - Coursera Course: Genomic and Precision Medicine
    - Training Residents in Genomics (TRIG) Working Group Genomic Pathology Workshop Handbook and Toolkit
  - 2B3: Recognize that genomic tests require interpretation with respect to the patient’s clinical status (e.g., pathogenic, likely pathogenic, benign)
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - Genetics in Primary Care Institute Webinar Series
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - DNA sequence nomenclature and variant interpretation
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - CAP’s Genomic Analysis Resource Guide
    - Coursera Course: Genomic and Precision Medicine
    - Training Residents in Genomics (TRIG) Working Group Genomic Pathology Workshop Handbook and Toolkit
  - 2B4: Explain the concepts of analytic validity, clinical validity, clinical utility as they relate to genomic testing
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - PDQ Cancer Information Summaries: Genetics
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - Training Residents in Genomics (TRIG) Working Group Genomic Pathology Workshop Handbook and Toolkit
  - 2B5: Recognize that medically ’non-actionable’ genomic results can be useful to the patient and family (i.e., personal utility)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - GEC KO
    - Training Residents in Genomics (TRIG) Working Group Genomic Pathology Workshop Handbook and Toolkit
- P-GT2C: Practice-Based Learning and Improvement
  - 2C1: Incorporate genomic findings into the health record and patient-care plan
    - NHGRI Genomics in Medicine Lecture Series
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Newborn Screening Fact Sheets
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - How to Build a Genetic Patient Registry
    - CAP’s Genomic Analysis Resource Guide
  - 2C2: Have a method for periodic review of ’new’ genomic interpretation for clinical applications.
    - NHGRI Genomics in Medicine Lecture Series
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care Institute Family History Tools
- P-GT2D: Interpersonal and Communication Skills
  - 2D1: Ensure that undergoing genomic testing is a joint decision of the patient and the physician
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Primary Care and Genetics and Genomics
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
  - 2D2: Explain and document findings from genomic testing to patient, including implications for other family members
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetic Medicine and Primary Care Infographic
    - Hereditary colorectal cancers
    - Primary Care and Genetics and Genomics
    - National Coalition for Health Professional Education (NCHPEG)
    - CAP’s Genomic Analysis Resource Guide
    - GEC KO
  - 2D3: Facilitate access to resources to enhance patient learning about the results of genomic testing
    - Medical Genetics in Pediatric Practice
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - American College of Obstetricians and Gynecologists Committee Opinion: Personalized Genomic Testing for Disease Risk
    - Primary Care and Genetics and Genomics
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - GEC KO
  - 2D4: Address the needs of the patient as an individual as well as the needs of family members
    - Medical Genetics in Pediatric Practice
    - Introduction to the Newborn Screening Fact Sheets
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care Institute Webinar Series
    - Primary Care and Genetics and Genomics
    - National Cancer Institute Understanding Cancer Series
- P-GT2E: Professionalism
  - 2E1: Be aware of and comply with local and federal laws and regulations regarding use of genomic tests
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American College of Obstetricians and Gynecologists Committee Opinion: Personalized Genomic Testing for Disease Risk
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - Primary Care and Genetics and Genomics
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
    - Coursera Course: Genomic and Precision Medicine
  - 2E2: Be aware of and responsive to patients’ concerns about genetic discrimination
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - Primary Care and Genetics and Genomics
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
    - GEC KO
  - 2E3: Respect patient’s privacy and need to maintain confidentiality of genomic information
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - Primary Care and Genetics and Genomics
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
    - GEC KO
- P-GT2F: Systems-Based Practice
  - 2F1: Explain who could have access to a patient’s genomic information
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - How to Build a Genetic Patient Registry
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
  - 2F2: Recognize the effects of the costs and coverage of genomic testing on utilization by patients
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Genetic Medicine and Primary Care Infographic
    - Genetics in Primary Care Institute Video Testimonials
    - Coding Fact Sheet for Genetics in Primary Care
    - Genetics in Primary Care Institute Webinar Series
    - Genetic Testing Reimbursement and Regulation…What You Need to Know
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
  - 2F3: Facilitate access of patients to relevant clinical studies or trials based on genomic testing
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
- P-GT2G: Interprofessional Collaboration
  - 2G1: Initiate responsible referrals to specialists or other health professionals
    - National Genetics and Genomics Education Centre (UK)
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - PDQ Cancer Information Summaries: Genetics
    - Introduction to the Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Genetic Medicine and Primary Care Infographic
    - Genetics in Primary Care Institute Family History Tools
    - American College of Obstetricians and Gynecologists Committee Opinion: Personalized Genomic Testing for Disease Risk
    - Genetics in Primary Care Institute Webinar Series
    - Quick Guide to Molecular Diagnostics
    - DNA from A to Z & Back Again
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - National Coalition for Health Professional Education (NCHPEG)
    - GEC KO
    - Family History in Cancer Risk Assessment, Testing and Management
  - 2G2: Provide support to patients based on recommendations of specialists
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - Quick Guide to Molecular Diagnostics
    - DNA from A to Z & Back Again
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Hereditary colorectal cancers
    - National Coalition for Health Professional Education (NCHPEG)
  - 2G3: Maintain a dialog with the clinical laboratory to ensure that the appropriate test(s) are ordered and interpreted in the context of the patient’s clinical status
    - Medical Genetics in Pediatric Practice
    - Ethical and Policy Issues in Genetic Testing and Screening of Children
    - Introduction to the Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - Genetics in Primary Care Institute Video Testimonials
    - Genetics in Primary Care Institute Webinar Series
    - Quick Guide to Molecular Diagnostics
    - DNA sequence nomenclature and variant interpretation
    - DNA from A to Z & Back Again
    - Hereditary pancreatitis
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Hereditary colorectal cancers
    - Genetic Testing Reimbursement and Regulation…What You Need to Know
    - National Coalition for Health Professional Education (NCHPEG)
    - CAP’s Genomic Analysis Resource Guide
- P-GT2H: Personal and Professional Development
  - 2H1: Engage in continuing education regarding advances in genomic medicine and changing indications for and interpretation of genomic testing
    - NHGRI Genomics in Medicine Lecture Series
    - Introduction to the Newborn Screening Fact Sheets
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Newborn Screening Fact Sheets
    - Genetics in Primary Care
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - American College of Obstetricians and Gynecologists Committee Opinion: Personalized Genomic Testing for Disease Risk
    - DNA from A to Z & Back Again
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
    - Association for Molecular Pathology (AMP) Molecular Genetic Pathology Online Self-Study Review Course
    - GEC KO
3: PATIENT TREATMENT BASED ON GENOMIC RESULTS
- P-PM3A: Patient Care
  - 3A1: Identify medical conditions and drug responses that have a strong genetic component
    - NHGRI Genomics in Medicine Lecture Series
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Genetics in Primary Care
    - Genetic Medicine and Primary Care Infographic
    - Coding Fact Sheet for Genetics in Primary Care
    - Genetics in Primary Care Institute Webinar Series
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - Hereditary pancreatitis
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Hereditary colorectal cancers
    - Warfarin pharmacogenetics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - Breast Cancer Clinical Recommendations
    - Colorectal Cancer
    - National Cancer Institute Understanding Cancer Series
    - Genetics
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
    - Orphanet
  - 3A2: Recognize that variants affecting drug responses found in a patient may also have implications for other family members
    - NHGRI Genomics in Medicine Lecture Series
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Genetics in Primary Care
    - Genetics in Primary Care Institute Family History Tools
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Introduction to pharmacogenetics
    - National Cancer Institute Understanding Cancer Series
    - Genetics
    - Association for Molecular Pathology (AMP) Webinar Series
  - 3A3: Discern the potential clinical impact of genetic variation on risk stratification and individualized treatment
    - NHGRI Genomics in Medicine Lecture Series
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Genetics in Primary Care
    - Genetic testing for hereditary breast cancer
    - Quick Guide to Molecular Diagnostics
    - Pharmacogenomics in pain management
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Warfarin pharmacogenetics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - National Cancer Institute Understanding Cancer Series
    - Genetics
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
- P-PM3B: Knowledge for Practice
  - 3B1: Appreciate the importance of genetic diversity of humans and the abundance of genetic variants in each individual genome
    - NHGRI Genomics in Medicine Lecture Series
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - Genetics in Primary Care
    - American College of Obstetricians and Gynecologists WEBTREATS: Genetics, Genomics, and the Human Genome Project
    - Pharmacogenomics in pain management
    - DNA sequence nomenclature and variant interpretation
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Introduction to pharmacogenetics
    - Primary Care and Genetics and Genomics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - National Cancer Institute Understanding Cancer Series
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
  - 3B2: Identify single-gene disorders that may be amenable to targeted pharmacological therapy
    - NHGRI Genomics in Medicine Lecture Series
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Genetics in Primary Care
    - Pharmacogenomics in pain management
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Introduction to pharmacogenetics
    - Primary Care and Genetics and Genomics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - National Cancer Institute Understanding Cancer Series
    - Association for Molecular Pathology (AMP) Webinar Series
  - 3B3: Recognize that genomic test results may guide choice of therapy for multifactorial disorders
    - NHGRI Genomics in Medicine Lecture Series
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Genetics in Primary Care
    - Pharmacogenomics in pain management
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - National Cancer Institute Understanding Cancer Series
    - Association for Molecular Pathology (AMP) Webinar Series
  - 3B4: Recognize that there is variability in the phenotypic expression of genetic variants and in response to therapy
    - NHGRI Genomics in Medicine Lecture Series
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Genetics in Primary Care
    - Pharmacogenomics in pain management
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Introduction to pharmacogenetics
    - Primary Care and Genetics and Genomics
    - Warfarin pharmacogenetics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - National Cancer Institute Understanding Cancer Series
    - Association for Molecular Pathology (AMP) Webinar Series
  - 3B5: Recognize that the effects of some medications are strongly influenced by inherited or somatically acquired genetic variation
    - NHGRI Genomics in Medicine Lecture Series
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Genetics in Primary Care
    - Pharmacogenomics in pain management
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Introduction to pharmacogenetics
    - Primary Care and Genetics and Genomics
    - Warfarin pharmacogenetics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
- P-PM3C: Practice-Based Learning and Improvement
  - 3C1: Use evidence-based recommendations of professional organizations and others in implementing knowledge gained from genetic discoveries to improve therapeutics
    - PharmGenEd
    - Pharmacogenomics: Increasing the safety and effectiveness of drug therapy (electronic brochure)
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Hereditary colorectal cancers
    - Warfarin pharmacogenetics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
  - 3C2: Document and periodically reassess therapeutic decision-making into the medical record of patients
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - How to Build a Genetic Patient Registry
  - 3C3: Incorporate a realistic assessment of personal genomic knowledge and skill in the selection and use of consultants and improve competencies in the wake of these interactions
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - PediaGene Smartphone / Tablet App
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - PDQ Cancer Information Summaries: Genetics
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Genetic Medicine and Primary Care Infographic
- P-PM3D: Interpersonal and Communication Skills
  - 3D1: Discuss benefits, risks, and alternatives of various preventive and therapeutic approaches driven by genomic findings
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Genetics in Primary Care
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Hereditary colorectal cancers
    - Primary Care and Genetics and Genomics
    - Warfarin pharmacogenetics
    - Association for Molecular Pathology (AMP) Webinar Series
  - 3D2: Communicate clearly with other medical professionals involved in the care of the patient about the therapeutic implications of the genetic information garnered about the patient 3D3. Discuss pharmacogenomics implications for future health
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - Medical Genetics in Pediatric Practice
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Genetics in Primary Care
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Primary Care and Genetics and Genomics
    - Association for Molecular Pathology (AMP) Webinar Series
  - 3D3: Discuss pharmacogenomics implications for future health
    - National Genetics and Genomics Education Centre (UK)
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Genetics in Primary Care
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Introduction to pharmacogenetics
    - Primary Care and Genetics and Genomics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - Association for Molecular Pathology (AMP) Webinar Series
- P-PM3E: Professionalism
  - 3E1: Respect and guard privacy of the patient and the family members
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - OMIM
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
- P-PM3F: Systems-Based Practice
  - 3F1: ’Treat the patient who has the disease’, i.e., be aware of the patient’s needs as an individual who also has a genetic disease or pharmacogenomic variation
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Coursera Course: Genomic and Precision Medicine
- P-PM3G: Interprofessional Collaboration
  - 3G1: Recognize potential involvement of multiple organ systems in genetic disorders and therefore appreciate the need to seek appropriate consultation with experts in the field
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
  - 3G2: Make medical and genetic information available to other health-care professionals, upon obtaining proper consent, while keeping the patients interests as the primary priority
    - PharmGenEd
    - Medical Genetics in Pediatric Practice
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - Genetics in Primary Care Institute Video Testimonials
    - Coding Fact Sheet for Genetics in Primary Care
- P-PM3H: Personal and Professional Development
  - 3H1: Maintain the medical knowledge and clinical competence in genomics required for the provision of therapy
    - PharmGenEd
    - Health Care Supervision for Children With Williams Syndrome
    - Health Supervision for Children With Achondroplasia
    - Health Supervision for Children With Down Syndrome
    - Health Supervision for Children With Fragile X Syndrome
    - Health Supervision for Children With Neurofibromatosis
    - Health Supervision for Children With Prader-Willi Syndrome
    - Health Supervision for Children With Marfan Syndrome
    - Health Supervision for Children with Sickle Cell Disease
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - Genetics in Primary Care
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Breast Cancer Clinical Recommendations
    - Colorectal Cancer
    - National Cancer Institute Understanding Cancer Series
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
    - Association for Molecular Pathology (AMP) Molecular Genetic Pathology Online Self-Study Review Course
  - 3H2: Be familiar with the available databases and resources relevant to genetic variation, including ongoing clinical trials involving patients with genetic disorders, pharmacogenomics, and patient-oriented Internet resources from reliable organizations
    - NHGRI Genomics in Medicine Lecture Series
    - PharmGenEd
    - Genetics in Primary Care
    - Genetics in Primary Care Institute Webinar Series
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Warfarin pharmacogenetics
    - Pharmacogenomics and the era of personalized medicine: essential phases of implementation and practical challenges
    - National Cancer Institute Understanding Cancer Series
    - Association for Molecular Pathology (AMP) Webinar Series
    - Orphanet
4: SOMATIC GENOMICS
- P-SG4A: Patient Care
  - 4A1: Identify or facilitate identification of patients who may benefit from genomic testing of tissue
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - PDQ Cancer Information Summaries: Genetics
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Detection of somatic mutations in tumors
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
  - 4A2: Explain the benefits and limitations of somatic genomic testing to the patient, including implications regarding treatment of their condition and clarification of his/her prognosis
    - PDQ Cancer Information Summaries: Genetics
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Detection of somatic mutations in tumors
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
  - 4A3: Ensure that tissue biopsy procedures are coordinated to make certain that appropriate and sufficient material is obtained for testing
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Detection of somatic mutations in tumors
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
  - 4A4: Integrate genomic testing results into the patient-care plan
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - PDQ Cancer Information Summaries: Genetics
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Detection of somatic mutations in tumors
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
- P-SG4B: Knowledge for Practice
  - 4B1: Explain the concept of somatic genetic change
    - My Cancer Genome: Genetically Informed Cancer Medicine
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - American College of Obstetricians and Gynecologists WEBTREATS: Genetics, Genomics, and the Human Genome Project
    - Massively parallel (Next-generation) sequencing primer
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Detection of somatic mutations in tumors
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - CAP’s Molecular Pathology Resource Guide
    - Training Residents in Genomics (TRIG) Working Group Genomic Pathology Workshop Handbook and Toolkit
  - 4B2: Describe the role of genomic changes in the pathophysiology and treatment of cancer
    - My Cancer Genome: Genetically Informed Cancer Medicine
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - Massively parallel (Next-generation) sequencing primer
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Detection of somatic mutations in tumors
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - CAP’s Molecular Pathology Resource Guide
    - Training Residents in Genomics (TRIG) Working Group Genomic Pathology Workshop Handbook and Toolkit
  - 4B3: Explain how genomic testing can be used to guide choice of therapy and adjust drug dosage in patients with cancer
    - PDQ Cancer Information Summaries: Genetics
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Massively parallel (Next-generation) sequencing primer
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Detection of somatic mutations in tumors
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - CAP’s Molecular Pathology Resource Guide
    - Coursera Course: Genomic and Precision Medicine
    - Training Residents in Genomics (TRIG) Working Group Genomic Pathology Workshop Handbook and Toolkit
- P-SG4C: Practice-Based Learning and Improvement
  - 4C1: Maintain an awareness of and follow evidence-based guidelines and other professional resources regarding somatic genetic disorders appropriate to the physician’s scope of practice
    - My Cancer Genome: Genetically Informed Cancer Medicine
    - PDQ Cancer Information Summaries: Genetics
    - Detection of somatic mutations in tumors
    - National Cancer Institute Cancer Risk Prediction and Assessment: Bibliography of Risk Prediction Models
    - National Coalition for Health Professional Education (NCHPEG)
    - Association for Molecular Pathology (AMP) Webinar Series
    - CAP’s Molecular Pathology Resource Guide
- P-SG4D: Interpersonal and Communication Skills
  - 4D1: Communicate to the patient the importance of genomic testing of his/her tissue sample, including potential implications for treatment and prognosis, and the limitations of genomic testing
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - My Cancer Genome: Genetically Informed Cancer Medicine
    - Detection of somatic mutations in tumors
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
  - 4D2: Address any concerns the patient may have about test results
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
    - CAP’s Molecular Pathology Resource Guide
  - 4D3: Ensure that specialists involved in a patients care are communicating with one another and with the patient
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
  - 4D4: Communicate to patients potential implications for his/her family
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - PDQ Cancer Information Summaries: Genetics
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - National Coalition for Health Professional Education (NCHPEG)
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
    - CAP’s Molecular Pathology Resource Guide
- P-SG4E: Professionalism
  - 4E1: Ensure that the patient is aware of what will happen with any tissue samples obtained
    - American College of Obstetricians and Gynecologists Committee Opinion: Ethical Issues in Genetic Testing
    - National Cancer Institute Understanding Cancer Series
    - Presidential Commission for the Study of Bioethical Issues: Community Engagement in Privacy and Progress in Whole Genome Sequencing
- P-SG4F: Systems-Based Practice
  - 4F1: Maintain a dialog with the clinical laboratory to ensure that the appropriate test(s) are ordered and interpreted in the context of the patient’s clinical status
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - DNA sequence nomenclature and variant interpretation
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - Detection of somatic mutations in tumors
    - Genetic Testing Reimbursement and Regulation…What You Need to Know
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
    - Association for Molecular Pathology (AMP) Molecular Genetic Pathology Online Self-Study Review Course
  - 4F2: Be prepared to refer patients to clinical trials designed to evaluate new approaches to cancer therapy
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - National Cancer Institute Understanding Cancer Series
    - Association for Molecular Pathology (AMP) Webinar Series
- P-SG4G: Interprofessional Collaboration
  - 4G1: Make appropriate referrals to specialists and other health providers and support the patient in ongoing care
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - PDQ Cancer Information Summaries: Genetics
    - American Society of Clinical Oncology: e-Learning Course: Genetic Testing in Oncology
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - National Cancer Institute Understanding Cancer Series
    - National Coalition for Health Professional Education (NCHPEG)
    - CAP’s Molecular Pathology Resource Guide
- P-SG4H: Personal and Professional Development
  - 4H1: Keep up-to-date with progress in the diagnosis and treatment of cancer and other tissue-based disorders
    - NHGRI Genomics in Medicine Lecture Series
    - Hereditary Colorectal Cancer: Is Your Patient at High Risk?
    - My Cancer Genome: Genetically Informed Cancer Medicine
    - American Society of Clinical Oncology: e-Learning Courses: Genetics and Genomics for the Practicing Clinician
    - American Society of Clinical Oncology: e-Learning Course: Cancer Genetics Review
    - Clinical Genomics: Practical Applications in Adult Patient Care
    - National Cancer Institute Cancer Risk Prediction and Assessment: Bibliography of Risk Prediction Models
    - Association for Molecular Pathology (AMP) Webinar Series
    - Coursera Course: Genomic and Precision Medicine
    - ASCO Cancer Genetics Program
5: MICROBIAL GENOMIC INFORMATION
- P-MG5A: Patient Care
  - 5A1: Use genomic-based tests for infectious disease instead of classical strategies where appropriate (e.g., based on clinical validity and turn-around time)
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
  - 5A2: Appreciate the sensitivity and specificity of genomics-based tests for diagnosis of infectious disease based on the clinical presentation, suspected pathogen type and testing method
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
  - 5A3: Interpret genomics-based tests for diagnosis, monitoring, and treatment of infectious disease
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
- P-MG5B: Knowledge for Practice
  - 5B1: Explain the core strategies for genomic testing for microbial disease
    - Association of Professors of Human and Medical Genetics (APHMG): MEDICAL SCHOOL CORE CURRICULUM IN GENETICS 2013
    - American College of Obstetricians and Gynecologists WEBTREATS: Genetics, Genomics, and the Human Genome Project
    - Clinical Genomics: Practical Applications in Adult Patient Care
  - 5B2: Describe how DNA or RNA sequence variations in the microbiome may predict response to therapy and clinical outcomes
    - Clinical Genomics: Practical Applications in Adult Patient Care
  - 5B3: Explain the potential reasons for false-positive and false-negative microbial genomic-based tests
    - Clinical Genomics: Practical Applications in Adult Patient Care
  - 5B4: Explain the importance of ’normal’ microbiome to health and disease
    - Clinical Genomics: Practical Applications in Adult Patient Care
- P-MG5C: Practice-Based Learning and Improvement
  - 5C1: Monitor ongoing testing results and their implications for treatment and prognosis in chronic infection
  - 5C2: Be aware of new genomic testing methods and their clinical applications and apply when appropriate
  - 5C3: Maintain awareness of patterns of infection in your patient population and use genomic tests appropriate to these patterns
- P-MG5D: Interpersonal and Communication Skills
  - 5D1: Explain the results of microbial genomic testing to patients
  - 5D2: Explain to patients and families results that signal a risk for contagion and take appropriate containment steps
- P-MG5E: Professionalism
  - 5E1: Provide guidance to patients on how to avoid transmission of microbial agents in the community
  - 5E2: Appreciate the importance of genomic tests for public health and responsibilities of primary-care physicians in reporting results to the appropriate public health authorities
- P-MG5F: Systems-Based Practice
  - 5F1: Work with other health-care professionals to apply infection-control measures when appropriate in both inpatient and outpatient settings
  - 5F2: Reassure patients and health-care workers in those situations in which ’infection control’ is not indicated
- P-MG5G: Interprofessional Collaboration
  - 5G1: Identify appropriate specialists and public health officials who need to be included in the care of the patient with infectious disease and function as a member of the care team
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
  - 5G2: Maintain a dialog with the clinical laboratory to ensure that the appropriate test(s) are ordered and interpreted in the context of the patient’s clinical status
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
  - 5G3: Consult with infectious disease specialists as needed (e.g., to manage unusual or unexpected infection or infection that is highly resistant to treatment)
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care
- P-MG5H: Personal and Professional Development
  - 5H1: Maintain up-to-date knowledge on genomic approaches to care for patients with microbial infection
    - Quick Guide to Molecular Diagnostics
    - Clinical Genomics: Practical Applications in Adult Patient Care