Disease association ontology term - MONDO:0008135 - optic atrophy 13 with retinal and foveal abnormalities

Term summary

ID: MONDO:0008135
Name: optic atrophy 13 with retinal and foveal abnormalities
Ontology or CV name: Disease association

Parents

is_a hereditary optic atrophy

Annotation

Disease association

MONDO:0008135 - optic atrophy 13 with retinal and foveal abnormalities

References:

PB_REF:0000006

Genes:

rim1 (SPAC2F3.04c)