Tetrahydrofolate methyltransferase deficiency

disorder

SNOMED 89579000CUI C0268611

Overview

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

Related Conditions

Enzymopathy(parent)

Disorder of sulphur-bearing amino acid metabolism(parent)

Inherited disorder of folate metabolism(parent)

Quick Facts

SNOMED CT: 89579000
UMLS CUI: C0268611
Fully Specified Name: Tetrahydrofolate methyltransferase 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.