American Board of Medical Genetics and Genomics
Rockville, MD 20852
Medical Genetics and Genomics
Medical geneticists specialize in medicine that involves the interaction between genes and health. They are trained to evaluate, diagnose, manage, treat and counsel individuals of all ages with hereditary disorders. This specialist uses modern cytogenetic, molecular, genomic and biochemical genetic testing to assist in specialized diagnostic evaluations, implement needed therapeutic interventions and provide genetic counseling and prevention through prenatal and preimplantation diagnosis. The Medical Geneticist plans and coordinates screening for genetic diseases involving single gene and chromosomal disorders, congenital anomalies, inborn errors of metabolism, multifactorial conditions, and common disorders with hereditary factors.
Training required prior to initial board certification
Two (2) to three (3) years
Board eligible period (+practice requirement)
Six (6) years
To become certified in a particular area of Medical Genetics and Genomics, a physician must complete specialized training before residency as specified by the Member Board.
Primary Specialty Certificates
Clinical Biochemical Genetics
A clinical biochemical geneticist demonstrates competence in directing and interpreting a wide range of specialized, laboratory biochemical genetic analyses relevant to the diagnosis and management of inherited metabolic disorders. The specialist acts as a consultant regarding laboratory diagnosis on a broad range of inborn errors of metabolism.
Clinical Genetics and Genomics (MD)
A clinical geneticist demonstrates competence in providing comprehensive diagnostic, management, therapeutic, and counseling services for individuals and families at risk for clinical disorders with a genetic basis. The specialist is trained to evaluate individuals of all ages for hereditary conditions.
Laboratory Genetics and Genomics
A diplomate certified in Laboratory Genetics and Genomics demonstrates competence in directing and interpreting both clinical cytogenetic and molecular genetic analyses relevant to the diagnosis and management of human genetic disease. This specialist acts as a consultant in laboratory diagnoses for a broad range of molecular and chromosomal-based disorders, including both inherited and acquired conditions.
To become certified in a particular subspecialty, a physician must complete additional training as specified by the Member Board.
Medical Biochemical Genetics
A medical biochemical geneticist demonstrates competence in the diagnosis, medical treatment and management of individuals with inherited metabolic conditions presenting clinically from infancy through adulthood, including via newborn screening. The subspecialist provides direct care and consultative care for individuals of all ages who are diagnosed with inborn errors of metabolism.
Molecular Genetic Pathology
A molecular genetic pathologist is expert in the principles, theory and technologies of molecular biology and molecular genetics. This expertise is used to make or confirm diagnoses of Mendelian genetic disorders, of human development, infectious diseases and malignancies and to assess the natural history of those disorders. A molecular genetic pathologist provides information about gene structure, function and alteration and applies laboratory techniques for diagnosis, treatment and prognosis for individuals with related disorders.
Lifelong learning requirements
- Effective in 2022, the literature review module or equivalent was deleted as this is covered through the longitudinal assessment activity.
- Complete one patient safety activity per 3-year cycle.
- Effective in 2022, complete 60 AMA PRA Category 1 Credits™ (or equivalent) CME credits throughout each 3-year cycle. At least 50% of the CME credits must be related to Medical Genetics and Genomics.