Disease #05499 (OPA5 (atrophy, optic, type 5 (OPA-5)), OMIM:610708)

Official abbreviation OPA5
Name atrophy, optic, type 5 (OPA-5)
OMIM ID 610708
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene DNM1L
Associated tissues -
Disease features autosomal dominant
Remarks -

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