Disease #04344 (OPA-8 (atrophy, optic?, type 8 (OPA-8)), OMIM:616289)

Official abbreviation OPA-8
Name atrophy, optic?, type 8 (OPA-8)
OMIM ID 616289
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ACO2
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited N/A