OMOP Concept 4033155
Hereditary gingival fibromatosis
StandardConditionSNOMED109620006Disorder
Maps from
2
Descendants
3
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Hereditary gingival fibromatosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562884 | Fibromatosis, Gingival, Hereditary | Non-standard |
| Nebraska Lexicon | 109620006 | Hereditary fibrous enlargement of gingiva | Non-standard |
Synonyms
Alternative names recorded for Hereditary gingival fibromatosis across source vocabularies.
- fibromatosis gingival hereditaria
- fibromatosis gingival hereditaria (trastorno)
- Hereditary fibrous enlargement of gingiva
- Hereditary gingival fibromatosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Digestive system hereditary disorder
- 1Gingival fibromatosis
- 1Non-plaque induced gingival disease
- 2Disorder of digestive system
- 2Fibromatosis
- 2Gingival disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of gingivae
- 3Digestive system finding
- 3Disease
- 3Disorder of body system
- 3Disorder of oral soft tissues
- 3Genetic disease
- 3Gingivae finding
- 3Lesion of soft tissue
- 3Oral lesion
- 3Periodontal disease
- 4Clinical finding
- 4Disease of mouth
- 4Disorder of digestive organ
- 4Disorder of soft tissue
- 4Disorder of soft tissue of head
- 4Disorder of teeth AND/OR supporting structures
Narrower concepts
(3)Included automatically when you query with descendants.
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