OMOP Concept 1244944
Type I interferonopathy
StandardConditionSNOMED1295193002Disorder
Maps from
0
Descendants
22
Valid from
1 Nov 2023
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Type I interferonopathy across source vocabularies.
- enfermedad autoinflamatoria asociada a interferón tipo I
- enfermedad autoinflamatoria asociada a interferón tipo I (trastorno)
- interferonopatía tipo 1
- interferonopatía tipo I
- Type 1 interferonopathy
- Type I interferon-associated autoinflammatory disease
- Type I interferon-associated autoinflammatory disease (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 1Monogenic autoinflammatory syndrome
- 2Autoinflammatory disease
- 2Genetic disease
- 3Disease
- 3Disorder of immune function
- 3Inflammatory disorder of immune system
- 4Clinical finding
- 4Disorder of immune structure
- 4Inflammation of specific body systems
- 5Disorder of body system
- 5Inflammation of specific body structures or tissue
- 6Inflammatory disorder
Narrower concepts
(22)Included automatically when you query with descendants.
- 1Aicardi Goutieres syndrome
- 1Autoimmune interstitial lung disease, arthritis syndrome
- 1Autosomal systemic lupus erythematosus
- 1Familial chilblain lupus erythematosus
- 1Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency
- 1Nakajo-Nishimura syndrome
- 1NOCARH syndrome
- 1Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
- 1SAMD9L-associated autoinflammatory syndrome
- 1Singleton-Merten syndrome
- 1Spondyloenchondrodysplasia
- 1STING-associated vasculopathy with onset in infancy
- 1Trichohepatoenteric syndrome
- 1USP18 deficiency
- 1Vasculitis due to adenosine deaminase 2 deficiency
- 1X-linked reticulate pigmentary disorder with systemic manifestation syndrome
- 2Aicardi Goutieres syndrome type 1
- 2Aicardi Goutieres syndrome type 2
- 2Aicardi Goutieres syndrome type 3
- 2Aicardi Goutieres syndrome type 4
- 2Aicardi Goutieres syndrome type 5
- 2Spondyloenchondrodysplasia with immune dysregulation
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