Overview
Congenital agammaglobulinemia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Autosomal agammaglobulinaemia with absent B-cells(child)
Swiss type agammaglobulinemia(child)
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome(child)
X-linked agammaglobulinemia with growth hormone deficiency(child)
Isolated agammaglobulinaemia(child)
BILU (B-cell immunodeficiency, limb, urogenital) syndrome(child)
Agammaglobulinemia due to SPI1 defect(child)
Autosomal recessive agammaglobulinaemia due to FNIP1 deficiency(child)
Congenital immunodeficiency disease(parent)
Quick Facts
- SNOMED CT
- 116133005
- UMLS CUI
- C5574711
- Fully Specified Name
- Congenital agammaglobulinemia (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.