Overview
Combined immunodeficiency disease is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Benign combined immunodeficiency(child)
Severe combined immunodeficiency disease(child)
Vici syndrome(child)
Absent thumb with short stature and immunodeficiency syndrome(child)
Combined immunodeficiency due to CRAC (calcium release activated calcium) channel dysfunction(child)
Immuno-osseous dysplasia(child)
Laron syndrome with immunodeficiency(child)
Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency(child)
Combined immunodeficiency due to OX40 deficiency(child)
Familial CD8 deficiency(child)
Roifman Chitayat syndrome(child)
Autosomal recessive lymphoproliferative disease(child)
Combined immunodeficiency due to STK4 deficiency(child)
FILS syndrome(child)
Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency(child)
Severe dermatitis, multiple allergies, metabolic wasting syndrome(child)
T-cell receptor alpha-beta-positive T-cell deficiency(child)
RIDDLE (radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties) syndrome(child)
Pancytopenia due to IKZF1 mutations(child)
Hyper-IgM syndrome with susceptibility to opportunistic infections(child)
Quick Facts
- SNOMED CT
- 442459007
- UMLS CUI
- C2711630
- Fully Specified Name
- Combined immunodeficiency disease (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.