HNSHA due to gamma glutamyl cysteine synthetase deficiency

disorder

SNOMED 25251008CUI C0272071

Overview

HNSHA due to gamma glutamyl cysteine synthetase deficiency is a disorder.

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

Related Conditions

Erythrocyte enzyme deficiency(parent)

Anemia due to enzyme deficiency(parent)

Hereditary nonspherocytic haemolytic anaemia(parent)

Quick Facts

SNOMED CT: 25251008
UMLS CUI: C0272071
Fully Specified Name: Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase 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.

HNSHA due to gamma glutamyl cysteine synthetase deficiency — Symptoms, Testing & Specialists | Ltrl