OMOP Concept 36715140
Cholestasis with pigmentary retinopathy and cleft palate syndrome
StandardConditionSNOMED720636001Disorder
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 Cholestasis with pigmentary retinopathy and cleft palate syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535632 | Hardikar syndrome | Non-standard |
Synonyms
Alternative names recorded for Cholestasis with pigmentary retinopathy and cleft palate syndrome across source vocabularies.
- Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder)
- Hardikar syndrome
- síndrome de colestasis con retinopatía pigmentaria y fisura de paladar
- síndrome de colestasis con retinopatía pigmentaria y fisura de paladar (trastorno)
- síndrome de Hardikar
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(103)Roll up to these when you need a wider cohort.
- 1Cholestasis
- 1Cleft palate with cleft lip
- 1Congenital anomaly of liver
- 1Congenital anomaly of retina
- 1Congenital malformation of the urinary system
- 1Multiple system malformation syndrome
- 1Retinal pigment deposits
- 2Cleft lip
- 2Cleft palate
- 2Congenital abnormality of liver and/or biliary tract
- 2Congenital anomaly of posterior segment of eye
- 2Congenital malformation syndrome
- 2Disorder of pigmentation
- 2Disorder of urinary system
- 2Genitourinary congenital anomalies
- 2Lesion of retina
- 2Liver finding
- 2Retinal deposits
- 2Retinal disorder
- 2Structural abnormality of liver
- 3Abdominal organ finding
- 3Anomaly of eye
- 3Congenital anomaly of abdomen
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of eye
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