Optic Atrophy 2 (OPA2)

Alias:

Opa2

Non-Leber Type Optic Atrophy with Early-Onset

Early-Onset X-Linked Optic Atrophy

Optic Atrophy, X-Linked

Optic Atrophy Type 2

Optic Atrophy, Non-Leber Type, with Early Onset

Optic Atrophy 2, X-Linked

X-Linked Optic Atrophy 2

Atrophy, Optic, Type 2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Optic Atrophy 2, also known as opa2, is related to optic atrophy 1 and 3-methylglutaconic aciduria, type iii. An important gene associated with Optic Atrophy 2 is OPA2 (Optic Atrophy 2 (Obscure)). Affiliated tissues include eye, and related phenotypes are optic atrophy and progressive visual loss

Related ID：

MALACARDS：OPT023

OMIM：311050