Human Genetics (also known as Genetics, Human): The scientific study of inherited human variation.

NIH MeSH · D000074705Disciplines and Occupations

Human Genetics

Also known asGenetics, Human

Definition

The scientific study of inherited human variation.

MeSH classification

  • H01.158.273.343.385

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Related concepts

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Gene Ontology

Sets of structured vocabularies used for describing and categorizing genes, and gene products by their molecular function, involvement in bi…

Genetic Research

Research into the cause, transmission, amelioration, elimination, or enhancement of inherited disorders and traits.

Genetics

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Genetics, Medical

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Common questions about Human Genetics

What does Human Genetics mean in medicine?
The scientific study of inherited human variation. This definition is taken from the National Library of Medicine's MeSH (Medical Subject Headings) 2026 release, which is the standard vocabulary used to index PubMed and most medical literature.
Is Human Genetics known by any other names?
Yes. Human Genetics is also referred to as Genetics, Human in different clinical, research and patient-facing contexts. The MeSH descriptor groups all of these synonyms under a single canonical concept so research and records stay consistent.
Where does Human Genetics sit in the medical classification?
Human Genetics falls under the broader medical category "Disciplines and Occupations" in the MeSH hierarchy (tree numbers: H01.158.273.343.385). Browsing the related concepts on this page takes you to neighbouring topics in the same branch of medicine.
Where can I get a plain-language explanation of Human Genetics?
For a plain-language explanation of Human Genetics - including symptoms, treatments and what it means for an Indian patient - ask GoDavaii's Health AI. It works in 22+ Indian languages, is free and needs no signup. Tap "Ask GoDavaii AI about Human Genetics" above.

Source: NIH MeSH 2026 (D000074705) — National Library of Medicine, public domain. View official MeSH record ↗