Carney Triad - CISMeF

Preferred Label : Carney Triad;

NCIt definition : An extremely rare syndrome characterized by the presence of gastrointestinal stromal tumors, pulmonary chondroma, and/or extra-adrenal paraganglioma. There is no evidence of familial inheritance.;

Alternative definition : NCI-GLOSS: A very rare disorder marked by tumors of the gastrointestinal tract (usually the stomach), tumors that form in embryonic nervous tissue in the head, neck, and torso, and tumors that form in cartilage in the lungs. Sometimes tumors also form in the adrenal glands and esophagus. Carney triad is most common in young females.;

Codes from synonyms : CDR0000648576;

Détails

Origin ID

C94833;

UMLS CUI

C1858592;

Automatic exact mappings (from CISMeF team)
- Carney syndrome [PASCAL descriptor]
Currated CISMeF NLP mapping
- Carney triad [ICD-11 More detail]
- Carney triad [OMIM Phenotype]
- Carney triad [ORDO Disease]
- Carney triad (disorder) [SNOMED CT concept]
- carney triad [MeSH concept]
- carney triad [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Carney triad [OMIM Phenotype]
- Carney triad [ORDO Disease]
- Carney triad (disorder) [SNOMED CT concept]
- carney triad [MeSH Supplementary Concept]
- carney triad [MeSH concept]

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

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