OMOP Concept 40483560
Combined immunodeficiency disease
StandardConditionSNOMED442459007Disorder
Maps from
26
Descendants
148
Valid from
31 Jul 2009
Valid to
31 Dec 2099
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Source codes that map to this concept
26 source codes normalize to Combined immunodeficiency disease via the OMOP "Maps to" relationship.
Showing 25 of 26 source codes. Retrieve the full set via the API.
Synonyms
Alternative names recorded for Combined immunodeficiency disease across source vocabularies.
- Combined immunodeficiency disease (disorder)
- enfermedad de inmunodeficiencia combinada
- enfermedad de inmunodeficiencia combinada (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
(148)Included automatically when you query with descendants.
- 1Absent thumb with short stature and immunodeficiency syndrome
- 1Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome
- 1Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
- 1Autosomal dominant combined immunodeficiency due to Aiolos deficiency
- 1Autosomal dominant combined immunodeficiency due to STAT5b mutation
- 1Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect
- 1Autosomal recessive combined immunodeficiency due to BCL10 mutation
- 1Autosomal recessive combined immunodeficiency due to CD28 mutation
- 1Autosomal recessive combined immunodeficiency due to CHUK mutation
- 1Autosomal recessive combined immunodeficiency due to COPG1 deficiency
- 1Autosomal recessive combined immunodeficiency due to ICOS deficiency
- 1Autosomal recessive combined immunodeficiency due to ICOSLG deficiency
- 1Autosomal recessive combined immunodeficiency due to ITPKB mutation
- 1Autosomal recessive combined immunodeficiency due to MAN2B2 mutation
- 1Autosomal recessive combined immunodeficiency due to MCM10 deficiency
- 1Autosomal recessive combined immunodeficiency due to PAX1 mutation
- 1Autosomal recessive combined immunodeficiency due to POLD1 mutation
- 1Autosomal recessive combined immunodeficiency due to POLD2 mutation
- 1Autosomal recessive combined immunodeficiency due to RELB mutation
- 1Autosomal recessive combined immunodeficiency due to REL mutation
- 1Autosomal recessive combined immunodeficiency due to WIP deficiency
- 1Autosomal recessive DNA repair defect due to LIG1 deficiency
- 1Autosomal recessive DNA repair defect due to POLE2 deficiency
- 1Autosomal recessive lymphoproliferative disease
- 1Benign combined immunodeficiency
Showing 25 of 148. Retrieve the full set via the API.
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