3-phosphoglycerate dehydrogenase deficiency infantile form

disorder

SNOMED 733637001CUI C4518085

Overview

3-phosphoglycerate dehydrogenase deficiency infantile form is a disorder.

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

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Inherited metabolic disorder of nervous system(parent)

3-Phosphoglycerate dehydrogenase deficiency(parent)

Developmental hereditary disorder(parent)

Congenital microcephalus(parent)

Quick Facts

SNOMED CT: 733637001
UMLS CUI: C4518085
Fully Specified Name: 3-phosphoglycerate dehydrogenase deficiency infantile form (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.