Disease #03967

Official abbreviation NDGOA
Name neurodegeneration, with optic atrophy, childhood-onset (NDGOA)
OMIM ID 615491
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene UCHL1
Associated tissues -
Disease features -
Remarks -