OMOP Concept 37204325
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome
StandardConditionSNOMED782949007Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536384 | FACES syndrome | Non-standard |
Synonyms
Alternative names recorded for Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome across source vocabularies.
- FACES (facial dysmorphism, anorexia, cachexia, eye and skin anomalies) syndrome
- Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder)
- Friedman Goodman syndrome
- síndrome de dismorfismo facial, anorexia, caquexia y anomalías oculares y cutáneas
- síndrome de dismorfismo facial, anorexia, caquexia y anomalías oculares y cutáneas (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(57)Roll up to these when you need a wider cohort.
- 1Café au lait spots
- 1Developmental hereditary disorder
- 1Fetal and/or neonatal disorder of integument
- 1Genetic disorder of skin pigmentation
- 1Hereditary disorder of the integument
- 1Multiple malformation syndrome with facial defects as major feature
- 1Retinitis pigmentosa
- 2Congenital anomaly of face
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of skin pigmentation
- 2Fetal and/or neonatal disorder
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary retinal dystrophy
- 2Multiple system malformation syndrome
- 3Congenital anomaly of head
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
- 3Disorder of face
- 3Disorder of pigmentation
- 3Hereditary disorder of the visual system
- 3Integumentary system finding
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