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Conditions / Genetic

digenic disease

info · Genetic

A polygenic disease that is characterized by expression of a phenotype that requires the presence of pathogenic variants in two different genes.

See it in the 3D body

This condition is mapped at the genetic level.

HumanAtlas is an educational atlas — not a medical device and not medical advice. See disclaimer. 3D anatomy: Z-Anatomy / BodyParts3D (CC BY-SA 4.0). Data: Disease Ontology (CC0), Human Phenotype Ontology, NLM RxNorm/RxClass, Wikipedia (CC BY-SA).