Disease #05499

Official abbreviation OPA-5
Name atrophy, optic, type 5 (OPA-5)
OMIM ID 610708
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DNM1L
Associated tissues -
Disease features autosomal dominant
Remarks -

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