OMOP Concept 4179930
Juvenile hemochromatosis
StandardConditionSNOMED50855007Disorder
Maps from
3
Descendants
2
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 Juvenile hemochromatosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136374 | Juvenile hemochromatosis | Non-standard |
| MeSH | C537247 | Hemochromatosis, type 2 | Non-standard |
| Nebraska Lexicon | 50855007 | Juvenile haemochromatosis | Non-standard |
Synonyms
Alternative names recorded for Juvenile hemochromatosis across source vocabularies.
- Haemochromatosis type 2
- Hemochromatosis type 2
- hemocromatosis juvenil
- hemocromatosis juvenil (trastorno)
- hemocromatosis tipo 2
- Juvenile haemochromatosis
- Juvenile hemochromatosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Hereditary hemochromatosis
- 2Autosomal hereditary disorder
- 2Hemochromatosis
- 2Hereditary metabolic disease
- 3Hereditary disease
- 3Iron overload
- 3Metabolic disease
- 4Disease
- 4Disorder of iron metabolism
- 4Genetic disease
- 4Mineral excess
- 5Clinical finding
- 5Disorder of mineral metabolism
- 5Excess intake of micronutrients
- 6Disorder of hyperalimentation
- 7Nutritional disorder
Narrower concepts
(2)Included automatically when you query with descendants.
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