OMOP Concept 36717770
Hemochromatosis type 4
StandardConditionSNOMED719975002Disorder
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 Hemochromatosis type 4 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537249 | Hemochromatosis, type 4 | Non-standard |
Synonyms
Alternative names recorded for Hemochromatosis type 4 across source vocabularies.
- Autosomal dominant hereditary haemochromatosis
- Autosomal dominant hereditary hemochromatosis
- Autosomal dominant hereditary hemochromatosis (disorder)
- Haemochromatosis due to defect in ferroportin
- Haemochromatosis type 4
- Hemochromatosis due to defect in ferroportin
- hemocromatosis debida a defecto de ferroportina
- hemocromatosis hereditaria autosómica dominante
- hemocromatosis hereditaria autosómica dominante (trastorno)
- hemocromatosis tipo 4
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 dominant 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
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