eccrine dermal cylindroma

Preferred Label : eccrine dermal cylindroma;

Details

Origin ID

M-82000;

UMLS CUI

C1305968;

Automatic exact mappings (from CISMeF team)
- Eccrine dermal cylindroma [ICD-11 Extension code]
- Turban tumor (morphologic abnormality) [SNOMED CT concept]
- Turban tumour [ICD-11 Extension code]
CISMeF manual mappings
- Cylindroma of skin (morphologic abnormality) [SNOMED CT concept]
- familial cylindromatosis [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Brooke Spiegler syndrome [Disease (Nov.)]
- Brooke-Spiegler syndrome [ORDO Disease]
- Brooke-Spiegler syndrome [DO Concept]
- Brooke-Spiegler syndrome [PASCAL descriptor]
- Brooke-Spiegler syndrome [MeSH concept]
- Brooke-Spiegler syndrome (disorder) [SNOMED CT concept]
- Brooke-spiegler syndrome [OMIM Phenotype]
- Cylindromatosis, familial [OMIM Phenotype]
- Eccrine dermal cylindroma (morphologic abnormality) [SNOMED CT concept]
- Eccrine dermal cylindroma of skin (disorder) [SNOMED CT concept]
- Familial cylindromatosis [ORDO Disease]
- Familial cylindromatosis [MeSH concept]
- Turban Tumor [NCIt concept]
- familial cylindromatosis [Disease (Nov.)]
ICD-10 exact mapping(s)
- Other malignant neoplasms of skin [ICD-10 category (who)]
Référence SNOMED
- scalp, nos [SNOMED Notion]
- skin, nos [SNOMED Notion]
SNOMED CT concept
- Eccrine dermal cylindroma (morphologic abnormality) [SNOMED CT concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Cylindroma [HPO term]
- Cylindroma [NCIt concept]
- 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 [MeSH concept]
- Familial cylindromatosis [ORDO Disease]
- familial cylindromatosis [MeSH Supplementary Concept]

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