Related Conditions
Reticular dysgenesis(child)
Severe combined immunodeficiency with reticular dysgenesis(child)
Shwachman syndrome(child)
X-linked severe congenital neutropenia(child)
Autosomal dominant severe congenital neutropaenia(child)
Severe congenital neutropenia type 3(child)
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Onycho-tricho-dysplasia neutropenia syndrome(child)
WHIM - Warts, hypogammaglobulinaemia, infections and myelokathexis(child)
Neutropenic disorder(parent)
Congenital immunodeficiency disease(parent)
Quick Facts
- SNOMED CT
- 89655007
- UMLS CUI
- C0340970
- Fully Specified Name
- Congenital neutropenia (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.