fibromatosis, congenital generalized

Preferred Label : fibromatosis, congenital generalized;

MeSH note : PROM;

MeSH synonym : myofibromatosis, infantile; Myofibromatosis, Juvenile;

Details

Origin ID

C562978;

UMLS CUI

C0432284;

Automatic exact mappings (from CISMeF team)
- Congenital generalised fibromatosis [ICD-11 Extension code]
- Infantile myofibromatosis [OMIM phenotypic series]
- Multicentric infantile myofibromatosis (disorder) [SNOMED CT concept]
- Myofibromatosis [NCIt concept]
- Myofibromatosis (morphologic abnormality) [SNOMED CT concept]
- myofibromatosis [SNOMED Notion]
Currated CISMeF NLP mapping
- Infantile myofibromatosis [PASCAL descriptor]
- Infantile myofibromatosis [ORDO Disease]
- Infantile myofibromatosis (disorder) [SNOMED CT concept]
- Myofibromatosis, infantile, 1 [OMIM Phenotype]
- infantile myofibromatosis [DO Concept]
- infantile myofibromatosis [Radlex concept]
MeSH term(s) associated for indexing
- myofibromatosis [MeSH Descriptor]
Record concept(s)
- fibromatosis, congenital generalized [MeSH concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital generalized fibromatosis (morphologic abnormality) [SNOMED CT concept]
- Infantile myofibromatosis [ORDO Disease]
- Infantile myofibromatosis [PASCAL descriptor]
- Infantile myofibromatosis (disorder) [SNOMED CT concept]
- Myofibromatosis, infantile, 1 [OMIM Phenotype]
- infantile fibromatosis [Disease (Nov.)]
- infantile myofibromatosis [DO Concept]
- infantile myofibromatosis [Radlex concept]
Validated automatic mappings to BTNT
- infantile fibromatosis [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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