Disease association ontology term - MONDO:0014889 - striatonigral degeneration, childhood-onset

Term summary

ID: MONDO:0014889
Name: striatonigral degeneration, childhood-onset
Ontology or CV name: Disease association

Parents

is_a striatonigral degeneration
is_a inherited dystonia

Annotation

Disease association

MONDO:0014889 - striatonigral degeneration, childhood-onset

References:

PB_REF:0000006

Genes:

vac14 (SPBC25H2.03)