Fibromatosis, gingival, 2

Preferred Label : Fibromatosis, gingival, 2;

Symbol : GINGF2;

CISMeF acronym : GGF2; GINGF2; HGF2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Fibromatosis, gingival, hereditary, 2; HGF2; GGF2;

Prefixed ID : %605544;

Details

Origin ID

605544;

UMLS CUI

C1854181;

Automatic exact mappings (from CISMeF team)
- NRG1 wt Allele [NCIt concept]
- gingival fibromatosis, hereditary, 2 [ORDO Gene]
- gingival fibromatosis, hereditary, 2 [HGNC gene]
Broader ORDO disease(s)
- Hereditary gingival fibromatosis [ORDO Disease]
Currated CISMeF NLP mapping
- fibromatosis, gingival, 2 [MeSH concept]
- fibromatosis, gingival, 2 [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, 2 [MeSH Supplementary Concept]
- fibromatosis, gingival, 2 [MeSH concept]
Validated automatic mappings to NTBT
- Hereditary gingival fibromatosis [ORDO Disease]

Keyword's position in hierarchy(ies) :

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