OMOP Concept 4147488
Acatalasemia
StandardConditionSNOMED267454002Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Acatalasemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 150490 | Acatalasaemia | Non-standard |
| MeSH | D020642 | Acatalasia | Non-standard |
| Nebraska Lexicon | 267454002 | Catalase deficiency | Non-standard |
| OXMIS | 2738AC | ACATALASIA | Non-standard |
| Read | C37y400 | Acatalasia | Non-standard |
Synonyms
Alternative names recorded for Acatalasemia across source vocabularies.
- Acatalasaemia
- acatalasemia
- Acatalasemia (disorder)
- acatalasemia (trastorno)
- acatalasia
- Acatalasia
- Catalase deficiency
- enfermedad de Takahara
- Takahara disease
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.
- 1Loss of single peroxisomal function
- 1Non-malignant white cell disorder
- 2Disorder of peroxisomal function
- 2White blood cell disorder
- 3Disorder of cellular component of blood
- 3Disorder of immune function
- 3Inborn error of metabolism
- 3OMOP Neutropenia 1
- 4Congenital disease
- 4Disease
- 4Finding of blood, lymphatics and immune system
- 4Hereditary metabolic disease
- 5Clinical finding
- 5Disorder of fetus and/or newborn
- 5Hereditary disease
- 5Metabolic disease
- 6Genetic disease
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