← Back to Conditions
Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect
disorderSNOMED 1351778007CUI C5968939
Overview
Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Thrombocytopenia due to immune destruction(parent)
Congenital immunodeficiency disease(parent)
Hereditary disorder of immune system(parent)
Hereditary thrombocytopenic disorder(parent)
Combined immunodeficiency disease(parent)
Congenital thrombocytopenia(parent)
Recessive hereditary disorder (autosomal)(parent)
Quick Facts
- SNOMED CT
- 1351778007
- UMLS CUI
- C5968939
- Fully Specified Name
- Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect (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.