OMOP Concept 607683
Progressive familial intrahepatic cholestasis type 1
StandardConditionSNOMED1155913007Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2021
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Progressive familial intrahepatic cholestasis type 1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535933 | Cholestasis, progressive familial intrahepatic 1 | Non-standard |
Synonyms
Alternative names recorded for Progressive familial intrahepatic cholestasis type 1 across source vocabularies.
- Byler syndrome
- CIFP1 - colestasis intrahepática familiar progresiva tipo 1
- colestasis intrahepática familiar progresiva tipo 1
- colestasis intrahepática familiar progresiva tipo 1 (trastorno)
- PFIC1 - progressive familial intrahepatic cholestasis type 1
- Progressive familial intrahepatic cholestasis type 1 (disorder)
- síndrome de Byler
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(39)Roll up to these when you need a wider cohort.
- 1Progressive intrahepatic cholestasis
- 2Autosomal recessive hereditary disorder
- 2Chronic liver disease
- 2Chronic metabolic disorder
- 2Digestive system hereditary disorder
- 2Disorder of biliary tract
- 2Disorder of bilirubin metabolism
- 2Intrahepatic cholestasis
- 2Metabolic and genetic disorder affecting the liver
- 3Autosomal hereditary disorder
- 3Cholestasis
- 3Chronic digestive system disorder
- 3Chronic disease
- 3Disease of liver
- 3Disorder of digestive system
- 3Disorder of liver and/or biliary tract
- 3Disorder of porphyrin metabolism
- 3Finding of biliary tract
- 3Hereditary disorder by system
- 3Metabolic disease
- 3OMOP Acute Liver Failure 1
- 4Digestive system finding
- 4Disease
- 4Disorder of abdomen
- 4Disorder of body system
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