Trichoepithelioma, multiple familial, 2

Preferred Label : Trichoepithelioma, multiple familial, 2;

CISMeF acronym : MFT2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MFT2;

Description : Multiple familial trichoepithelioma (MFT) is an autosomal dominant disorder of skin appendage tumors characterized by the appearance of trichoepitheliomas. See also MFT1 (601606), which is caused by mutations in the CYLD gene (605018) on chromosome 16q12-q13.;

Prefixed ID : %612099;

Details

Origin ID

612099;

UMLS CUI

C2677505;

Currated CISMeF NLP mapping
- trichoepithelioma, multiple familial, 2 [MeSH concept]
- trichoepithelioma, multiple familial, 2 [MeSH Supplementary Concept]
ORDO concept(s)
- Brooke-Spiegler syndrome [ORDO Disease]
- Familial multiple trichoepithelioma [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- trichoepithelioma, multiple familial, 2 [MeSH Supplementary Concept]
- trichoepithelioma, multiple familial, 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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