hypertrichosis terminalis, generalized, with or without gingival hyperplasia

Preferred Label : hypertrichosis terminalis, generalized, with or without gingival hyperplasia;

MeSH synonym : microdeletion 17q24.2-q24.3 syndrome; chromosome 17q24.2-q24.3 deletion syndrome; fibromatosis, gingival, with hypertrichosis;

Details

Origin ID

C565016;

UMLS CUI

C1851120;

Automatic exact mappings (from CISMeF team)
- Gingival fibromatosis - hypertrichosis [ICD-11 More detail]
CISMeF manual mappings
- Gingival fibromatosis-hypertrichosis syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Gingival fibromatosis and hypertrichosis syndrome (disorder) [SNOMED CT concept]
- Hypertrichosis, congenital generalized, with or without gingival hyperplasia [OMIM Phenotype]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosomes, human, pair 17 [MeSH Descriptor]
- fibromatosis, gingival [MeSH Descriptor]
- hypertrichosis [MeSH Descriptor]
Record concept(s)
- hypertrichosis terminalis, generalized, with or without gingival hyperplasia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Gingival fibromatosis-hypertrichosis syndrome [ORDO Disease]
- Hypertrichosis, congenital generalized, with or without gingival hyperplasia [OMIM Phenotype]

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