OMOP Concept 36714657
Hemochromatosis type 3
StandardConditionSNOMED719974003Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Hemochromatosis type 3 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537248 | Hemochromatosis, type 3 | Non-standard |
| Nebraska Lexicon | 719974003 | Haemochromatosis type 3 | Non-standard |
Synonyms
Alternative names recorded for Hemochromatosis type 3 across source vocabularies.
- Haemochromatosis type 3
- Hemochromatosis type 3 (disorder)
- hemocromatosis tipo 3
- hemocromatosis tipo 3 (trastorno)
- TFR2 (transferrin receptor 2 gene) related haemochromatosis
- TFR2 (transferrin receptor 2 gene) related hemochromatosis
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
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