HNSHA due to hexokinase deficiency

disorder

SNOMED 42484009CUI C0272063

Overview

HNSHA due to hexokinase deficiency is a disorder.

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

Related Conditions

Erythrocyte enzyme deficiency(parent)

Autosomal hereditary disorder(parent)

Anemia due to enzyme deficiency(parent)

Inborn error of metabolism(parent)

Hereditary nonspherocytic haemolytic anaemia(parent)

Hemolytic anemia due to hexokinase deficiency(parent)

Congenital anemia(parent)

Quick Facts

SNOMED CT: 42484009
UMLS CUI: C0272063
Fully Specified Name: Hereditary nonspherocytic hemolytic anemia due to hexokinase 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.