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Homozygous methylenetetrahydrofolate reductase mutation

disorder
SNOMED 139811000119109CUI C3875381

Overview

Homozygous methylenetetrahydrofolate reductase mutation is a disorder.

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

Related Conditions

Hereditary disorder of endocrine system(parent)
Congenital disease(parent)

Quick Facts

SNOMED CT
139811000119109
UMLS CUI
C3875381
Fully Specified Name
Homozygous methylenetetrahydrofolate reductase mutation (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.