OMOP Concept 36716201
Overgrowth, macrocephaly, facial dysmorphism syndrome
StandardConditionSNOMED722122000Disorder
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 Overgrowth, macrocephaly, facial dysmorphism syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 722122000 | Overgrowth, macrocephaly, facial dysmorphism syndrome | Non-standard |
Synonyms
Alternative names recorded for Overgrowth, macrocephaly, facial dysmorphism syndrome across source vocabularies.
- Overgrowth, macrocephaly, facial dysmorphism syndrome (disorder)
- Ring finger protein 135 related overgrowth syndrome
- RNF135 (ring finger protein 135) related overgrowth syndrome
- síndrome de crecimiento excesivo, macrocefalia, dismorfismo facial
- síndrome de crecimiento excesivo, macrocefalia, dismorfismo facial (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(26)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital macrocephaly
- 1Developmental hereditary disorder
- 1Multiple malformation syndrome with early overgrowth
- 1Multiple malformation syndrome with facial defects as major feature
- 2Autosomal hereditary disorder
- 2Congenital anomaly of face
- 2Congenital anomaly of head
- 2Developmental disorder
- 2Hereditary disease
- 2Macrocephaly
- 2Multiple system malformation syndrome
- 3Congenital malformation
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of face
- 3Disorder of head
- 3Finding of head circumference
- 3Genetic disease
- 4Body measurement finding
- 4Clinical finding
- 4Congenital disease
- 4Finding of face
- 4Head finding
- 5Disorder of fetus and/or newborn
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