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Conditions / Genetic

optic atrophy 4

info · Genetic

An optic atrophy that has_material_basis_in heterozygous mutation in a region on chromosome 18q12.2-q12.3.

Also known as: OPA4

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).