Parkinson disease 3 (autosomal dominant, Lewy body)

Preferred Label : Parkinson disease 3 (autosomal dominant, Lewy body);

Obsolete resource : true;

Approved symbol HGNC : PARK3;

Chromosome HGNC : 2p13;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:8608;

UMLS CUI

C1418271;

Automatic exact mappings (from CISMeF team)
- Parkinson disease 3, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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