HNSHA due to diphosphoglycerate mutase deficiency

disorder

SNOMED 62268000CUI C0272069

Overview

HNSHA due to diphosphoglycerate mutase deficiency is a disorder.

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

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Erythrocyte enzyme deficiency(parent)

Anemia due to enzyme deficiency(parent)

Hereditary nonspherocytic haemolytic anaemia(parent)

Quick Facts

SNOMED CT: 62268000
UMLS CUI: C0272069
Fully Specified Name: Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase 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.