Disease association ontology term - MONDO:0015003 - dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities

Term summary

ID: MONDO:0015003
Name: dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
Ontology or CV name: Disease association

Parents

is_a inherited lipoic acid biosynthesis defect
is_a inherited neurodegenerative disorder
is_a inherited dystonia

Annotation

Disease association

MONDO:0015003 - dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities

References:

PB_REF:0000006

Genes:

etr1 (SPAC26F1.04c)