OMOP Concept 4239314
Primary immune deficiency disorder
StandardConditionSNOMED58606001Disorder
Maps from
2
Descendants
492
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Primary immune deficiency disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 129104 | Primary Immune Deficiency Disorder | Non-standard |
| MeSH | D000081207 | Primary Immunodeficiency Diseases | Non-standard |
Synonyms
Alternative names recorded for Primary immune deficiency disorder across source vocabularies.
- deficiencia inmunológica primaria
- deficiencia inmunológica primaria (trastorno)
- Primary immune deficiency disorder (disorder)
- Primary immunodeficiency
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(492)Included automatically when you query with descendants.
- 1Activated PI3K-delta syndrome
- 1Anhidrotic ectodermal dysplasia with immune deficiency
- 1Autoimmune lymphoproliferative syndrome
- 1Autosomal dominant predisposition to severe viral infection due to TLR3 deficiency
- 1Autosomal dominant predisposition to severe viral infection due to TRAF3 deficiency
- 1Autosomal recessive predisposition to severe viral infection due to TLR3 deficiency
- 1Autosomal recessive predisposition to severe viral infection due to UNC93B1 deficiency
- 1Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
- 1Blau syndrome
- 1CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome
- 1Combined immunodeficiency disease
- 1Common variable immunodeficiency
- 1Constitutional mismatch repair deficiency syndrome
- 1Deficiency in anterior pituitary function, variable immunodeficiency syndrome
- 1Deficiency of interleukin 36 receptor antagonist
- 1Disorder of complement
- 1Disorder of immunoglobulin
- 1Early-onset autoimmunity, autoinflammation, immunodeficiency syndrome due to SOCS1 haploinsufficiency
- 1Familial hyperinflammatory lymphoproliferative immunodeficiency
- 1Hyperimmunoglobulin M syndrome
- 1IL21-related infantile inflammatory bowel disease
- 1Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome
- 1Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome
- 1Immunodeficiency associated with chromosomal abnormality
- 1Immunodeficiency due to CD25 deficiency
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