Overview
Erythrocyte enzyme deficiency is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
CNSHA - Chronic non-spherocytic haemolytic anaemia(child)
PGK - Phosphoglycerokinase deficiency(child)
Glucose phosphate isomerase deficiency(child)
Triose phosphate isomerase deficiency(child)
Uridine monophosphate hydrolase deficiency(child)
Adenosine deaminase overproduction(child)
HNSHA due to glutathione synthetase deficiency(child)
Deficiency of glucose-6-phosphate dehydrogenase(child)
Deficiency of hexokinase type IV(child)
Hereditary stomatocytosis(child)
HNSHA due to gamma glutamyl cysteine synthetase deficiency(child)
HNSHA due to pyrimidine-5'-nucleotidase deficiency(child)
HNSHA due to phosphofructokinase deficiency(child)
HNSHA due to hexokinase deficiency(child)
HNSHA due to triosephosphate isomerase deficiency(child)
HNSHA due to NADH diaphorase deficiency(child)
HNSHA due to phosphoglycerate kinase deficiency(child)
HNSHA due to diphosphoglycerate mutase deficiency(child)
HNSHA due to decreased adenosine deaminase activity(child)
Deficiency of glutathione reductase (NAD(P)H)(child)
Quick Facts
- SNOMED CT
- 234401000
- UMLS CUI
- C0398558
- Fully Specified Name
- Erythrocyte enzyme 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.