Methylene THF reductase deficiency AND homocystinuria

disorder

SNOMED 28093001CUI C0268610

Overview

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

Related Conditions

Inherited disorder of folate metabolism(parent)

Recessive hereditary disorder (autosomal)(parent)

Enzymopathy(parent)

Homocystinuria(parent)

Quick Facts

SNOMED CT: 28093001
UMLS CUI: C0268610
Fully Specified Name: Methylene tetrahydrofolate methyltransferase reductase deficiency AND homocystinuria (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.