Terminology Service for NFDI4Health
Parkinson's disease 1
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http://purl.obolibrary.org/obo/DOID_0060367
A late onset Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein gene on chromosome 4q22.1. [ http://purl.obolibrary.org/obo/ECO_0007645 http://purl.obolibrary.org/obo/ECO_0007636 ]
Term info
Label
Parkinson's disease 1
Synonyms
- autosomal dominant Parkinson disease 1
- autosomal dominant Parkinson's disease 1
Subsets
DO_rare_slim
created by
elvira
creation date
2015-09-17T16:48:14Z
has obo namespace
disease_ontology
id
DOID:0060367