Congenital monosaccharide malabsorption

disorder

SNOMED 450849003CUI C3472585

Overview

Congenital monosaccharide malabsorption is a disorder.

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

Related Conditions

Disorder of carbohydrate absorption(parent)

Congenital disease(parent)

Malabsorption syndrome(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Quick Facts

SNOMED CT: 450849003
UMLS CUI: C3472585
Fully Specified Name: Congenital monosaccharide malabsorption (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.