Disease association ontology term - MONDO:0010774 - striatonigral degeneration, infantile, mitochondrial

Term summary

ID: MONDO:0010774
Name: striatonigral degeneration, infantile, mitochondrial
Ontology or CV name: Disease association

Parents

is_a familial infantile bilateral striatal necrosis

Annotation

Disease association

MONDO:0010774 - striatonigral degeneration, infantile, mitochondrial

References:

PB_REF:0000003

Genes:

atp6 (SPMIT.07)