autosomal dominant Parkinson disease 4
late onset Parkinson disease that has material basis in heterozygous triplication of the alpha-synuclein gene (SNCA) on chromosome 4q22
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autosomal dominant Parkinson disease 4
Summary
autosomal dominant Parkinson disease 4 is a rare disease[1].
Key Facts
- autosomal dominant Parkinson disease 4's instance of is recorded as rare disease[2].
- autosomal dominant Parkinson disease 4's instance of is recorded as class of disease[3].
- autosomal dominant Parkinson disease 4's subclass of is recorded as hereditary late onset Parkinson disease[4].
- autosomal dominant Parkinson disease 4's subclass of is recorded as autosomal dominant disease[5].
- autosomal dominant Parkinson disease 4's MeSH descriptor ID is recorded as C565324[6].
- autosomal dominant Parkinson disease 4's OMIM ID is recorded as 605543[7].
- autosomal dominant Parkinson disease 4's Disease Ontology ID is recorded as DOID:0060895[8].
- autosomal dominant Parkinson disease 4's NCI Thesaurus ID is recorded as C198604[9].
- autosomal dominant Parkinson disease 4's health specialty is recorded as neurology[10].
- autosomal dominant Parkinson disease 4's genetic association is recorded as SNCA[11].
- autosomal dominant Parkinson disease 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060895[12].
- autosomal dominant Parkinson disease 4's exact match is recorded as http://identifiers.org/doid/DOID:0060895[13].
- autosomal dominant Parkinson disease 4's UMLS CUI is recorded as C1854182[14].
- autosomal dominant Parkinson disease 4's ICD-10-CM is recorded as G20[15].
- autosomal dominant Parkinson disease 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- autosomal dominant Parkinson disease 4's Mondo ID is recorded as MONDO_0011562[17].
- autosomal dominant Parkinson disease 4's UniProt disease ID is recorded as DI-02135[18].