OMOP Concept 36715001
Acromegaloid facial appearance syndrome
StandardConditionSNOMED720456009Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Acromegaloid facial appearance syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535655 | Acromegaloid facial appearance syndrome | Non-standard |
| Nebraska Lexicon | 720456009 | Acromegaloid facial appearance syndrome | Non-standard |
Synonyms
Alternative names recorded for Acromegaloid facial appearance syndrome across source vocabularies.
- Acromegaloid facial appearance syndrome (disorder)
- síndrome de apariencia facial acromegaloide
- síndrome de apariencia facial acromegaloide (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of hand
- 1Developmental hereditary disorder
- 1Multiple malformation syndrome with facial-limb defects as major feature
- 2Autosomal hereditary disorder
- 2Congenital anomaly of limb
- 2Congenital anomaly of upper limb
- 2Developmental disorder
- 2Disorder of hand
- 2Hereditary disease
- 2Multiple malformation syndrome with facial defects as major feature
- 2Multiple malformation syndrome with limb defect as major feature
- 3Congenital anomaly of face
- 3Congenital malformation
- 3Disease
- 3Disorder of limb
- 3Disorder of upper limb
- 3Finding of hand region
- 3Genetic disease
- 3Multiple system malformation syndrome
- 4Clinical finding
- 4Congenital anomaly of head
- 4Congenital disease
- 4Congenital malformation syndrome
- 4Disorder of face
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