Gigantiform cementoma, familial

Preferred Label : Gigantiform cementoma, familial;

Symbol : FGC;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Cemental dysplasia, periapical; Cementomas, familial multiple;

Inheritance : Autosomal dominant;

Prefixed ID : %137575;

Details

Origin ID

137575;

UMLS CUI

C3495361;

Automatic exact mappings (from CISMeF team)
- Cementoma, NOS [ICD-11 Extension code]
- Familial gigantiform cementoma [MedDRA Preferred Term]
- Familial ossifying fibroma [ORDO Disease]
- Florid cemento-osseous dysplasia [ORDO Disease]
- Gigantiform cementoma (morphologic abnormality) [SNOMED CT concept]
Currated CISMeF NLP mapping
- gigantiform cementoma, familial [MeSH concept]
- gigantiform cementoma, familial [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Cementoma [HPO term]
- Multiple impacted teeth [HPO term]
- Tooth malposition [HPO term]
ORDO concept(s)
- Familial ossifying fibroma [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Familial gigantiform cementoma [MedDRA Preferred Term]
- Florid Cemento-Osseous Dysplasia [NCIt concept]
- Gigantiform Cementoma [NCIt concept]
- Gigantiform cementoma (morphologic abnormality) [SNOMED CT concept]
- gigantiform cementoma [SNOMED Notion]
- gigantiform cementoma, familial [MeSH Supplementary Concept]
- gigantiform cementoma, familial [MeSH concept]
Validated automatic mappings to NTBT
- Cementoma (morphologic abnormality) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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