autosomal dominant Parkinson disease 8
Parkinson's disease that has material basis in heterozygous mutation in the dardarin encoding gene (LRRK2) on chromosome 12q12
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autosomal dominant Parkinson disease 8
Summary
autosomal dominant Parkinson disease 8 is a rare disease[1].
Key Facts
- autosomal dominant Parkinson disease 8's instance of is recorded as rare disease[2].
- autosomal dominant Parkinson disease 8's instance of is recorded as class of disease[3].
- autosomal dominant Parkinson disease 8's subclass of is recorded as hereditary late onset Parkinson disease[4].
- autosomal dominant Parkinson disease 8's subclass of is recorded as autosomal dominant disease[5].
- autosomal dominant Parkinson disease 8's OMIM ID is recorded as 607060[6].
- autosomal dominant Parkinson disease 8's Disease Ontology ID is recorded as DOID:0060371[7].
- autosomal dominant Parkinson disease 8's NCI Thesaurus ID is recorded as C198605[8].
- autosomal dominant Parkinson disease 8's genetic association is recorded as LRRK2[9].
- autosomal dominant Parkinson disease 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060371[10].
- autosomal dominant Parkinson disease 8's exact match is recorded as http://identifiers.org/doid/DOID:0060371[11].
- autosomal dominant Parkinson disease 8's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_411602[12].
- autosomal dominant Parkinson disease 8's UMLS CUI is recorded as C1846862[13].
- autosomal dominant Parkinson disease 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant Parkinson disease 8's Mondo ID is recorded as MONDO_0011764[15].
- autosomal dominant Parkinson disease 8's UniProt disease ID is recorded as DI-02136[16].