Disease association ontology term - MONDO:0007429 - optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy

Term summary

ID: MONDO:0007429
Name: optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
Ontology or CV name: Disease association

Parents

is_a autosomal dominant optic atrophy plus syndrome

Annotation

Disease association

MONDO:0007429 - optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy

References:

PB_REF:0000006

Genes:

msp1 (SPBC1718.06)