Carney complex, type 2

Preferred Label : Carney complex, type 2;

Symbol : CNC2;

CISMeF acronym : CNC2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Carney myxoma-endocrine complex, type 2;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of Carney complex, see CNC1 (160980), which is caused by mutation in the PRKAR1A gene (188830) on chromosome 17q.;

Prefixed ID : %605244;

Détails

Origin ID

605244;

UMLS CUI

C1854540;

Automatic exact mappings (from CISMeF team)
- Carney complex [DO Concept]
- Carney complex type 2, multiple neoplasia and lentiginosis [HGNC gene]
- carney complex [MeSH Descriptor]
Currated CISMeF NLP mapping
- Carney complex type 2 [Disease (Nov.)]
- carney complex, type 2 [MeSH concept]
DO Cross reference
- Carney complex [DO Concept]
ORDO concept(s)
- Carney complex [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Carney complex type 2 [Disease (Nov.)]
- carney complex, type 2 [MeSH concept]

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

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