Fibromatosis, gingival, 3

Preferred Label : Fibromatosis, gingival, 3;

Symbol : GINGF3;

CISMeF acronym : GGF3; GINGF3; HGF3;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Fibromatosis, gingival, hereditary, 3; GGF3; HGF3;

Description : For phenotypic information and a discussion of genetic heterogeneity of hereditary gingival fibromatosis, see GINGF (135300).;

Prefixed ID : %609955;

Details

Origin ID

609955;

UMLS CUI

C1864960;

Broader ORDO disease(s)
- Hereditary gingival fibromatosis [ORDO Disease]
Currated CISMeF NLP mapping
- Fibromatosis, gingival, 3 [MeSH concept]
- fibromatosis, gingival, 3 [MeSH Supplementary Concept]
DO Cross reference
- gingival fibromatosis [DO Concept]
ORDO concept(s)
- Hereditary gingival fibromatosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fibromatosis, gingival, 3 [MeSH concept]
- fibromatosis, gingival, 3 [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- Hereditary gingival fibromatosis [ORDO Disease]

Keyword's position in hierarchy(ies) :

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