Parkinson disease 17
late-onset Parkinson disease that has material basis in heterozygous mutation in the VPS35 gene on chromosome 16q13
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Parkinson disease 17
Summary
Parkinson disease 17 is a rare disease[1].
Key Facts
- Parkinson disease 17's instance of is recorded as rare disease[2].
- Parkinson disease 17's instance of is recorded as class of disease[3].
- Parkinson disease 17's subclass of is recorded as hereditary late onset Parkinson disease[4].
- Parkinson disease 17's subclass of is recorded as genetic disease[5].
- Parkinson disease 17's OMIM ID is recorded as 614203[6].
- Parkinson disease 17's Disease Ontology ID is recorded as DOID:0060897[7].
- Parkinson disease 17's NCI Thesaurus ID is recorded as C201520[8].
- Parkinson disease 17's genetic association is recorded as VPS35[9].
- Parkinson disease 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060897[10].
- Parkinson disease 17's exact match is recorded as http://identifiers.org/doid/DOID:0060897[11].
- Parkinson disease 17's UMLS CUI is recorded as C3280133[12].
- Parkinson disease 17's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Parkinson disease 17's Mondo ID is recorded as MONDO_0013625[14].
- Parkinson disease 17's UniProt disease ID is recorded as DI-03242[15].