SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Monogenic autoinflammatory syndrome  724593005

Type I interferonopathy   1295193002

SNOMED CT code


SNOMED code1295193002
nameType I interferonopathy
statusactive
date introduced2023-11-01
fully specified name(s)Type I interferon–associated autoinflammatory disease (disorder)
synonyms
  • Type I interferonopathy
  • Type I interferon–associated autoinflammatory disease
  • Type 1 interferonopathy
attributes - group1
Finding siteImmune system structure   116003000
Associated morphologyInflammatory morphology   409774005
Pathological processAbnormal immune process   769247005
parentsMonogenic autoinflammatory syndrome   724593005
children
  • Aicardi Goutieres syndrome   230312006
  • STING-associated vasculopathy with onset in infancy   711164003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Monogenic autoinflammatory syndrome   724593005
          Type I interferonopathy   1295193002

ancestors
sorted most to least specific
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