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
  • UMLS:C3810053 (OMIM:615593)
  • OMIM:615593 (Orphanet:431149)
  • SCTID:766879006 (MONDO:equivalentTo)
  • ICD10:D81.8 (Orphanet:431149)
  • Orphanet:431149 (OMIM:615593)
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

http://identifiers.org/omim/615593

http://linkedlifedata.com/resource/umls/id/C3810053

http://identifiers.org/snomedct/766879006

http://www.orpha.net/ORDO/Orphanet_431149

has exact synonym

combined immunodeficiency with impaired immunity to HHV-8

immunodeficiency type 16

combined immunodeficiency with childhood-onset Kaposi sarcoma

combined immunodeficiency with impaired immunity to human herpes virus 8

has related synonym

immunodeficiency 16

OX40 deficiency

IMD16

id

MONDO:0014268