OMOP Concept 4180159
Hereditary disorder of immune system
StandardConditionSNOMED363138005Disorder
Maps from
0
Descendants
218
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Hereditary disorder of immune system across source vocabularies.
- Hereditary disorder of immune system (disorder)
- trastorno hereditario del sistema inmune
- trastorno hereditario del sistema inmunitario
- trastorno hereditario del sistema inmunitario (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(218)Included automatically when you query with descendants.
- 1Absent thumb with short stature and immunodeficiency syndrome
- 1Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
- 1Aicardi Goutieres syndrome
- 1Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation
- 1Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB GOF mutation
- 1Ataxia-telangiectasia syndrome
- 1Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome
- 1Autoimmune interstitial lung disease, arthritis syndrome
- 1Autoimmune lymphoproliferative syndrome
- 1Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
- 1Autoinflammation with arthritis and dyskeratosis due to NLRP1 deficiency
- 1Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
- 1Autosomal dominant combined variable immunodeficiency due to IRF2BP2 mutation
- 1Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation
- 1Autosomal dominant combined variable immunodeficiency due to SEC61A1 mutation
- 1Autosomal dominant combined variable immunodeficiency due to TWEAK mutation
- 1Autosomal recessive agammaglobulinemia due to FNIP1 deficiency
- 1Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect
- 1Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency
- 1Autosomal recessive combined immunodeficiency due to WIP deficiency
- 1Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation
- 1Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency
- 1Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation
- 1Autosomal recessive common variable immunodeficiency due to CD20 mutation
- 1Autosomal recessive common variable immunodeficiency due to CD21 mutation
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