Terminology Service for NFDI4Health
Parkinson's disease 2
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http://purl.obolibrary.org/obo/DOID_0060368
An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27. [ http://purl.obolibrary.org/obo/ECO_0007645 ]
Term info
Label
Parkinson's disease 2
Synonyms
- autosomal recessive juvenile Parkinson disease 2
- autosomal recessive juvenile Parkinson's disease 2
Subsets
DO_rare_slim
created by
elvira
creation date
2015-09-17T16:56:33Z
has obo namespace
disease_ontology
id
DOID:0060368