OMOP Concept 36714449
Gingival fibromatosis with facial dysmorphism syndrome
StandardConditionSNOMED719687007Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Gingival fibromatosis with facial dysmorphism syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719687007 | Gingival fibromatosis with facial dysmorphism syndrome | Non-standard |
Synonyms
Alternative names recorded for Gingival fibromatosis with facial dysmorphism syndrome across source vocabularies.
- fibromatosis gingival con síndrome de dismorfismo facial
- fibromatosis gingival con síndrome de dismorfismo facial (trastorno)
- Gingival fibromatosis with facial dysmorphism syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(49)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Disorder of digestive system specific to fetus OR newborn
- 1Hereditary gingival fibromatosis
- 1Multiple malformation syndrome with facial defects as major feature
- 2Autosomal hereditary disorder
- 2Congenital anomaly of face
- 2Developmental disorder
- 2Digestive system hereditary disorder
- 2Disorder of digestive system
- 2Disorder of fetus and/or newborn
- 2Gingival fibromatosis
- 2Hereditary disease
- 2Multiple system malformation syndrome
- 2Non-plaque induced gingival disease
- 3Congenital anomaly of head
- 3Congenital malformation syndrome
- 3Digestive system finding
- 3Disease
- 3Disorder of body system
- 3Disorder of face
- 3Fibromatosis
- 3Genetic disease
- 3Gingival disease
- 3Hereditary disorder by system
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