Parkinson disease 12

Preferred Label : Parkinson disease 12;

Symbol : PARK12;

CISMeF acronym : PARK12;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Parkinson disease, X-linked;

Description : For a phenotypic description and a discussion of genetic heterogeneity of Parkinson disease, see 168600.;

Prefixed ID : %300557;

Détails

Origin ID

300557;

UMLS CUI

C1845165;

Currated CISMeF NLP mapping
- parkinson disease 12 [MeSH concept]
- parkinson disease 12 [MeSH Supplementary Concept]
ORDO concept(s)
- Young-onset Parkinson disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- parkinson disease 12 [MeSH Supplementary Concept]
- parkinson disease 12 [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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