autosomal dominant Parkinson disease 1
human disease
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autosomal dominant Parkinson disease 1
Summary
autosomal dominant Parkinson disease 1 is a class of disease[1].
Key Facts
- autosomal dominant Parkinson disease 1's instance of is recorded as class of disease[2].
- autosomal dominant Parkinson disease 1's subclass of is recorded as hereditary late onset Parkinson disease[3].
- autosomal dominant Parkinson disease 1's subclass of is recorded as autosomal dominant disease[4].
- autosomal dominant Parkinson disease 1's MeSH descriptor ID is recorded as C566823[5].
- autosomal dominant Parkinson disease 1's OMIM ID is recorded as 168601[6].
- autosomal dominant Parkinson disease 1's Disease Ontology ID is recorded as DOID:0060367[7].
- autosomal dominant Parkinson disease 1's NCI Thesaurus ID is recorded as C198602[8].
- autosomal dominant Parkinson disease 1's genetic association is recorded as SNCA[9].
- autosomal dominant Parkinson disease 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060367[10].
- autosomal dominant Parkinson disease 1's exact match is recorded as http://identifiers.org/doid/DOID:0060367[11].
- autosomal dominant Parkinson disease 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_171695[12].
- autosomal dominant Parkinson disease 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_411602[13].
- autosomal dominant Parkinson disease 1's UMLS CUI is recorded as C1868596[14].
- autosomal dominant Parkinson disease 1's UMLS CUI is recorded as C1868595[15].
- autosomal dominant Parkinson disease 1's UMLS CUI is recorded as C3149705[16].
- autosomal dominant Parkinson disease 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- autosomal dominant Parkinson disease 1's Mondo ID is recorded as MONDO_0008200[18].
- autosomal dominant Parkinson disease 1's UniProt disease ID is recorded as DI-01223[19].