Disease #05194 (OPA10 (atrophy, optic, type 10, with/without ataxia, mental retardation, and seizures (OPA-10)), OMIM:616732)

Official abbreviation OPA10
Name atrophy, optic, type 10, with/without ataxia, mental retardation, and seizures (OPA-10)
OMIM ID 616732
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease 1
Associated with 1 gene RTN4IP1
Associated tissues eyes
Disease features -
Remarks -
Date created 2016-10-11 11:01:00 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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