Disease association ontology term - MONDO:0012466 - Parkinson disease 13, autosomal dominant, susceptibility to
Term summary
- ID
- MONDO:0012466
- Name
- Parkinson disease 13, autosomal dominant, susceptibility to
- Ontology or CV name
- Disease association
- Definition
- An inherited susceptibility or predisposition to developing young-onset Parkinson disease, in which the cause of the disease is a mutation in the HTRA2 gene.
