Genetics Healthcare Taxonomy Code 207SM0001X
HealthProviders DB is a comprehensive database of healthcare providers, including a complete directory of all Molecular Genetic Pathologists.
As of today, the following are the total number of Molecular Genetic Pathologists nationally, in your state, and near your location.
Medicare
The following are the total number of Molecular Genetic Pathologists who accept Medicare in your state, the number who have opted out of Medicare, and the total number excluded from participation in Medicare nationwide.
Alaska – Alabama – Armed Forces Pacific – Arkansas – American Samoa – Arizona – California – Colorado – Connecticut – District of Columbia – Delaware – Florida – Federated States of Micronesia – Georgia – Guam – Hawaii – Iowa – Idaho – Illinois – Indiana – Kansas – Kentucky – Louisiana – Massachusetts – Maryland – Maine – Marshall Islands – Michigan – Minnesota – Missouri – Northern Mariana Islands – Mississippi – Montana – North Carolina – North Dakota – Nebraska – New Hampshire – New Jersey – New Mexico – Nevada – New York – Ohio – Oklahoma – Oregon – Pennsylvania – Puerto Rico – Palau – Rhode Island – South Carolina – South Dakota – Tennessee – Texas – Utah – Virginia – Virgin Islands – Vermont – Washington – Wisconsin – West Virginia – Wyoming
Select the State name above or from the HealthProviders DB App filter panel to show the list of Molecular Genetic Pathologists by State. In addition, you can also narrow the list by City and more from the filter panel.
You can download the Molecular Genetic Pathology Medical Genetics Physicians dataset using HealthProviders DB Export.

What do Molecular Genetic Pathologists do?
Molecular Genetic Pathology physicians diagnose and interpret genetic disorders by analyzing genetic material to identify mutations.
They apply molecular biology and genetics to make or confirm diagnoses, determine prognosis, and guide treatment, especially in areas like cancer, where they help select targeted therapies.
Their work involves using laboratory techniques to study gene function and alteration, providing crucial information to other physicians for optimal patient care.
What they do
Supporting primary physicians: They provide information to primary care physicians so they can better care for patients with genetic conditions.
Diagnosing genetic diseases: They use laboratory techniques to diagnose and confirm inherited disorders, infectious diseases, and cancers by analyzing genetic material for mutations and alterations.
Confirming clinical diagnoses: They provide definitive diagnoses for conditions such as single-gene disorders, disorders of human development, and malignancies.
Interpreting genomic data: They interpret findings from genomic analysis to help physicians choose the most effective treatments, particularly for cancer patients with specific genetic mutations.
Assessing disease progression: They evaluate the natural history of a disorder to understand how it may progress over time.
Providing information for treatment and prognosis: They provide information about gene structure, function, and alteration to help guide treatment and predict the outcome of a disease.