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Disease association ontology term - MONDO:0014796 - autosomal recessive early-onset Parkinson disease 23

Term summary

ID
MONDO:0014796
Name
autosomal recessive early-onset Parkinson disease 23
Ontology or CV name
Disease association
Definition
Any young-onset Parkinson disease in which the cause of the disease is a mutation in the VPS13C gene.

Parents

Annotation

Disease association

MONDO:0014796 - autosomal recessive early-onset Parkinson disease 23

References:

Genes: