Fibromatosis, gingival, with progressive deafness

Preferred Label : Fibromatosis, gingival, with progressive deafness;

CISMeF acronym : GFD;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Jones syndrome; GFD; Gingival fibromatosis with sensorineural hearing loss;

Inheritance : Autosomal dominant;

Prefixed ID : %135550;

Details

Origin ID

135550;

UMLS CUI

C1851112;

Automatic exact mappings (from CISMeF team)
- Gingival fibromatosis - progressive deafness [ICD-11 More detail]
Currated CISMeF NLP mapping
- Gingival fibromatosis with progressive deafness syndrome (disorder) [SNOMED CT concept]
- Gingival fibromatosis-progressive deafness syndrome [ORDO Disease]
- Jones syndrome [MeSH concept]
- jones syndrome [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Gingival fibromatosis [HPO term]
- Progressive sensorineural hearing impairment [HPO term]
ORDO concept(s)
- Gingival fibromatosis-progressive deafness syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Gingival fibromatosis with progressive deafness syndrome (disorder) [SNOMED CT concept]
- Gingival fibromatosis-progressive deafness syndrome [ORDO Disease]
- Jones syndrome [MeSH concept]
- jones syndrome [MeSH Supplementary Concept]

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