OMOP Concept 4261471
Adenosine deaminase deficiency
StandardConditionSNOMED44940001Disorder
Maps from
13
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
13 source codes normalize to Adenosine deaminase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 149429 | Adenosine deaminase deficiency | Non-standard |
| CIM10 | D81.3 | Adenosine deaminase [ADA] deficiency | Non-standard |
| ICD10 | D81.3 | Adenosine deaminase [ADA] deficiency | Non-standard |
| ICD10CM | D81.3 | Adenosine deaminase [ADA] deficiency | Non-standard |
| ICD10CM | D81.30 | Adenosine deaminase deficiency, unspecified | Non-standard |
| ICD10CM | D81.31 | Severe combined immunodeficiency due to adenosine deaminase deficiency | Non-standard |
| ICD10CM | D81.39 | Other adenosine deaminase deficiency | Non-standard |
| ICD10CN | D81.3 | Adenosine deaminase [ADA] deficiency | Non-standard |
| ICD10CN | D81.300 | Adenosine deaminase [ADA] deficiency | Non-standard |
| ICD10GM | D81.3 | Adenosine deaminase [ADA] deficiency | Non-standard |
| KCD7 | D81.3 | Adenosine deaminase[ADA] deficiency | Non-standard |
| Read | C30yy11 | Adenosine-deaminase deficiency | Non-standard |
| Read | C392600 | Adenosine deaminase deficiency | Non-standard |
Synonyms
Alternative names recorded for Adenosine deaminase deficiency across source vocabularies.
- ADA - Adenosine aminohydrolase deficiency
- ADA deficiency
- Adenosine aminohydrolase deficiency
- Adenosine deaminase deficiency (disorder)
- deficiencia de ADA
- deficiencia de adenosina aminohidrolasa
- deficiencia de adenosina desaminasa
- deficiencia de adenosina desaminasa (trastorno)
- Deficiency of adenosine deaminase
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Autosomal recessive SCID (severe combined immunodeficiency disease)
- 1Disorder of purine metabolism
- 1Specific enzyme deficiency
- 2Autosomal recessive hereditary disorder
- 2Disorder of purine and pyrimidine metabolism
- 2Enzymopathy
- 2Severe combined immunodeficiency disease
- 3Autosomal hereditary disorder
- 3Combined immunodeficiency disease
- 3Congenital immunodeficiency disease
- 3Hereditary disorder of immune system
- 3Metabolic disease
- 4Congenital disease
- 4Disease
- 4Disorder of immune function
- 4Hereditary disease
- 4Hereditary disorder by system
- 4Immunodeficiency disorder
- 4Primary immune deficiency disorder
- 5Clinical finding
- 5Disorder of body system
- 5Fetal and/or neonatal disorder
- 5Genetic disease
Narrower concepts
(1)Included automatically when you query with descendants.
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