Trehalose intolerance

disorder

SNOMED 84193000CUI C0268187

Overview

Trehalose intolerance is a disorder.

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal circulating enzyme concentration or activity

Very frequent (80-99%)HP:0012379

Abdominal swelling

Occasional (5-29%)HP:0003270

Diarrhea

Occasional (5-29%)HP:0002014

Gastro pain

Occasional (5-29%)HP:0002027

Intestinal malabsorption

Occasional (5-29%)HP:0002024

Vomiting

Occasional (5-29%)HP:0002013

Related Conditions

Disorder of carbohydrate transport(parent)

Disorder of carbohydrate absorption(parent)

Inborn error of metabolism(parent)

Specific enzyme deficiency(parent)

Autosomal hereditary disorder(parent)

Quick Facts

SNOMED CT: 84193000
UMLS CUI: C0268187
Fully Specified Name: Trehalase deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.