Atypical haemolytic uraemic syndrome with complement gene abnormality

disorder

SNOMED 1293264009CUI C5680166

Overview

Atypical haemolytic uraemic syndrome with complement gene abnormality is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Atypical HUS (hemolytic uremic syndrome) with anti-CFH (complement factor H) Ab(child)

Thrombocytopenia due to immune destruction(parent)

Disorder of immune structure(parent)

Urinary complication(parent)

Atypical haemolytic uraemic syndrome(parent)

Quick Facts

SNOMED CT: 1293264009
UMLS CUI: C5680166
Fully Specified Name: Atypical hemolytic uremic syndrome with complement gene abnormality (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.