HNSHA due to triosephosphate isomerase deficiency

disorder

SNOMED 44641000CUI C0272067

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Anemia due to enzyme deficiency(parent)

Erythrocyte enzyme deficiency(parent)

Autosomal dominant hereditary disorder(parent)

Hereditary nonspherocytic haemolytic anaemia(parent)

Quick Facts

SNOMED CT: 44641000
UMLS CUI: C0272067
Fully Specified Name: Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase 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.