OMOP Concept 4123239
Immunodeficiency associated with chromosomal abnormality
StandardConditionSNOMED234632005Disorder
Maps from
1
Descendants
23
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Immunodeficiency associated with chromosomal abnormality via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 234632005 | Immunodeficiency associated with chromosomal abnormality | Non-standard |
Synonyms
Alternative names recorded for Immunodeficiency associated with chromosomal abnormality across source vocabularies.
- Immunodeficiency associated with chromosomal abnormality (disorder)
- inmunodeficiencia asociada a anomalía cromosómica
- inmunodeficiencia asociada a anomalía cromosómica (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(23)Included automatically when you query with descendants.
- 1Ataxia-telangiectasia syndrome
- 1Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome
- 1Autoimmune lymphoproliferative syndrome with recurrent viral infection
- 1Bloom syndrome
- 1Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
- 1Chromosome 18 syndromes and antibody deficiency
- 1Chromosome 22 abnormalities with hypogammaglobulinemia
- 1Combined immunodeficiency due to OX40 deficiency
- 1Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
- 1Deletion of X-chromosome and hypogammaglobulinemia
- 1FADD-related immunodeficiency
- 1Idiopathic CD4 lymphocytopenia
- 1Immunodeficiency associated with 18p syndrome
- 1Immunodeficiency due to ficolin 3 deficiency
- 1Microcephaly, normal intelligence and immunodeficiency
- 1Neutrophil immunodeficiency syndrome
- 1Primary immunodeficiency syndrome due to p14 deficiency
- 1Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency
- 1Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
- 1RAS-associated autoimmune leukoproliferative disease
- 1Triple X syndrome, epilepsy, and hypogammaglobulinemia
- 1X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome
- 2Monosomy 22 and absence of immunoglobulin A
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