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