Familial cylindromatosis

Preferred Label : Familial cylindromatosis;

UMLS semantic type : T047 - Disease or Syndrome; T191 - Neoplastic Process;

Origin ID

M0531072;

UMLS CUI

C1305968;

Currated CISMeF NLP mapping
- Brooke Spiegler syndrome [Disease (Nov.)]
- Brooke-Spiegler Syndrome [NCIt concept]
- Brooke-Spiegler syndrome [ORDO Disease]
- Brooke-Spiegler syndrome [DO Concept]
- Brooke-Spiegler syndrome [PASCAL descriptor]
- Brooke-spiegler syndrome [OMIM Phenotype]
- Cylindromatosis, familial [OMIM Phenotype]
- Eccrine dermal cylindroma of skin (disorder) [SNOMED CT concept]
- Familial cylindromatosis [ORDO Disease]
- eccrine dermal cylindroma [SNOMED Notion]
- familial cylindromatosis [Disease (Nov.)]
MeSH narrower concept(s)
- Trichoepithelioma multiple familial [MeSH concept]
Related MeSH concept(s)
- Brooke-Spiegler syndrome [MeSH concept]
Related record
- familial cylindromatosis [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Brooke-Spiegler syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Cylindroma [NCIt concept]
- Cylindroma [HPO term]
- Cylindroma of skin (morphologic abnormality) [SNOMED CT concept]
- Cylindromatosis, familial [OMIM Phenotype]
- Dermal cylindroma [MedDRA LLT]
- Eccrine dermal cylindroma (morphologic abnormality) [SNOMED CT concept]
- Eccrine dermal cylindroma of skin (disorder) [SNOMED CT concept]
- Familial cylindromatosis [ORDO Disease]
- eccrine dermal cylindroma [SNOMED Notion]