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Disease association ontology term - MONDO:0011658 - autosomal recessive early-onset Parkinson disease 7

Term summary

ID
MONDO:0011658
Name
autosomal recessive early-onset Parkinson disease 7
Ontology or CV name
Disease association
Definition
Any Parkinson disease in which the cause of the disease is a mutation in the PARK7 gene.

Parents

Annotation

Disease association

MONDO:0011658 - autosomal recessive early-onset Parkinson disease 7

References:

Genes: