OMOP Concept 4207656
Hepatic porphyria
StandardConditionSNOMED55056006Disorder
Maps from
3
Descendants
11
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Hepatic porphyria via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138825 | Hepatic porphyria | Non-standard |
| MeSH | D017094 | Porphyrias, Hepatic | Non-standard |
| Nebraska Lexicon | 55056006 | Hepatic porphyria | Non-standard |
Synonyms
Alternative names recorded for Hepatic porphyria across source vocabularies.
- Hepatic porphyria (disorder)
- porfiria hepática
- porfiria hepática (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Disease of liver
- 1Porphyria
- 2Disorder of liver and/or biliary tract
- 2Disorder of porphyrin metabolism
- 2Liver finding
- 2OMOP Acute Liver Failure 1
- 2OMOP Acute Liver Failure 2
- 2OMOP Acute Liver Failure 8
- 3Abdominal organ finding
- 3Digestive system finding
- 3Disorder of abdomen
- 3Disorder of digestive organ
- 3Metabolic disease
- 4Clinical finding
- 4Disease
- 4Disorder of abdominopelvic segment of trunk
- 4Disorder of digestive system
- 4Finding of abdomen
- 4Viscus structure finding
- 5Disorder of body system
- 5Disorder of trunk
- 5Finding of abdominopelvic segment of trunk
- 6Finding of trunk structure
Narrower concepts
(11)Included automatically when you query with descendants.
- 1Exacerbation of hepatic porphyria
- 1Hereditary coproporphyria
- 1Porphyria cutanea tarda
- 1Variegate porphyria
- 2Acquired porphyria cutanea tarda
- 2Erythropoietic coproporphyria
- 2Familial porphyria cutanea tarda
- 2Homozygous hereditary coproporphyria
- 2Homozygous porphyria cutanea tarda
- 2Homozygous variegate porphyria
- 2Sporadic porphyria cutanea tarda
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