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Autosomal recessive combined immunodeficiency due to WIPF1 mutation
disorderSNOMED 1351776006CUI C5968935
Overview
Autosomal recessive combined immunodeficiency due to WIPF1 mutation is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Combined immunodeficiency disease(parent)
Recessive hereditary disorder (autosomal)(parent)
Thrombocytopenia due to immune destruction(parent)
Congenital immunodeficiency disease(parent)
Hereditary disorder of immune system(parent)
Hereditary thrombocytopenic disorder(parent)
Congenital thrombocytopenia(parent)
Quick Facts
- SNOMED CT
- 1351776006
- UMLS CUI
- C5968935
- Fully Specified Name
- Autosomal recessive combined immunodeficiency due to Wiskott Aldrich syndrome protein-interacting protein deficiency (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.