" /> Optic atrophy 5 - CISMeF





Preferred Label : Optic atrophy 5;

Symbol : OPA5;

CISMeF acronym : OPA5;

Type : Phenotype, molecular basis known;

Description : For a discussion of genetic heterogeneity of optic atrophy, see OPA1 (165500).;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the dynamin 1-like gene (DNM1L, 603850.0009);

Prefixed ID : #610708;

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01/11/2024


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