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Combined immunodeficiency due to OX40 deficiency
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.
ORPHA:431149
Classification level: Disorder- Synonym(s):
- 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
- Prevalence: <1 / 1 000 000
- Inheritance: Autosomal recessive
- Age of onset: Childhood
- ICD-10: D81.8
- OMIM: 615593
- UMLS: C4707864
- MeSH: -
- GARD: -
- MedDRA: -
A summary on this disease is available in Deutsch (2018) Español (2018) Italiano (2018) Nederlands (2018)
Detailed information
Guidelines
- Clinical practice guidelines
- Français (2022) - PNDS


Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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