Overview
Autosomal recessive hyper-IgM syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
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Autosomal recessive hyperimmunoglobulin M syndrome due to APRIL deficiency(child)
Autosomal recessive hyperimmunoglobulin M syndrome due to CTNNBL1 deficiency(child)
Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency(child)
Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 deficiency(child)
Hyperimmunoglobulin M syndrome type 3(child)
Hyperimmunoglobulin M syndrome(parent)
Recessive hereditary disorder (autosomal)(parent)
Quick Facts
- SNOMED CT
- 403836001
- UMLS CUI
- C1275128
- Fully Specified Name
- Autosomal recessive hyperimmunoglobulin M syndrome (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.