OMOP Concept 4121109
Congenital deficiency of intrinsic factor
StandardConditionSNOMED234361004Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Congenital deficiency of intrinsic factor via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144050 | Congenital intrinsic factor deficiency | Non-standard |
| MeSH | C563242 | Intrinsic Factor Deficiency | Non-standard |
| Nebraska Lexicon | 234361004 | Congenital deficiency of intrinsic factor | Non-standard |
| Read | D010.13 | Congenital deficiency of intrinsic factor | Non-standard |
Synonyms
Alternative names recorded for Congenital deficiency of intrinsic factor across source vocabularies.
- Congenital deficiency of intrinsic factor (disorder)
- deficiencia congénita de factor intrínseco
- deficiencia congénita de factor intrínseco (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Congenital disease
- 1Pernicious anemia
- 2Disorder of fetus and/or newborn
- 2Megaloblastic anemia due to vitamin B-12 deficiency
- 3Disease
- 3Megaloblastic anemia
- 3Nutritional anemia
- 3Nutritional deficiency associated condition
- 4Anemia
- 4Anemia related to disturbed DNA synthesis
- 4Clinical finding
- 4Macrocytic anemia
- 5Disorder of cellular component of blood
- 6Finding of blood, lymphatics and immune system
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