OMOP Concept 4049879
Deficiency of histidine ammonia-lyase
StandardConditionSNOMED124628005Disorder
Maps from
3
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
3 source codes normalize to Deficiency of histidine ammonia-lyase via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 142707 | Deficiency of histidine ammonia-lyase | Non-standard |
| Nebraska Lexicon | 124628005 | Deficiency of histidine ammonia-lyase | Non-standard |
| Read | C305000 | Histidinaemia | Non-standard |
Synonyms
Alternative names recorded for Deficiency of histidine ammonia-lyase across source vocabularies.
- deficiencia de histidasa
- deficiencia de histidina a - deaminasa
- deficiencia de histidina amoníaco - liasa
- deficiencia de histidina amoníaco - liasa (trastorno)
- deficiencia de histidinasa
- Deficiency of histidase
- Deficiency of histidinase
- Deficiency of histidine a-deaminase
- Deficiency of histidine ammonia-lyase (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
- 1Disorder of histidine metabolism
- 1Inborn error of metabolism
- 1Specific enzyme deficiency
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Disorder of amino acid and organic acid metabolism
- 2Enzymopathy
- 2Hereditary metabolic disease
- 3Disorder of amino acid metabolism
- 3Disorder of fetus and/or newborn
- 3Hereditary disease
- 3Metabolic disease
- 4Disease
- 4Disorder of organic acid metabolism
- 4Genetic disease
- 5Clinical finding
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