combined immunodeficiency due to OX40 deficiency

Go to external page http://purl.obolibrary.org/obo/MONDO_0014268


Combined immunodeficiency due to OX40 deficiency is a rare combined T and B cell immunodeficiency characterized by susceptibility to develop an aggressive, childhood-onset, disseminated, cutaneous and systemic Kaposi sarcoma. [ Orphanet : 431149 ]

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:615593 (Orphanet:431149/e)
  • Orphanet:431149 (OMIM:615593)
  • UMLS:C3810053 (OMIM:615593)
  • SCTID:766879006 (MONDO:equivalentTo)
  • ICD10CM:D81.8 (Orphanet:431149/ntbt)
Subsets

ordo_disease

definition
  • Combined immunodeficiency due to OX40 deficiency is a rare combined T and B cell immunodeficiency characterized by susceptibility to develop an aggressive, childhood-onset, disseminated, cutaneous and systemic Kaposi sarcoma.
exactMatch
  • https://omim.org/entry/615593
  • http://linkedlifedata.com/resource/umls/id/C3810053
  • http://www.orpha.net/ORDO/Orphanet_431149
  • http://identifiers.org/snomedct/766879006
has exact synonym
  • combined immunodeficiency with childhood-onset Kaposi sarcoma
  • combined immunodeficiency with impaired immunity to HHV-8
  • combined immunodeficiency with impaired immunity to human herpes virus 8
  • immunodeficiency type 16
has related synonym
  • OX40 deficiency
  • immunodeficiency 16
  • IMD16
id
  • MONDO:0014268
narrowMatch
  • http://apps.who.int/classifications/icd10/browse/2010/en#/D81.8