Chronic diarrhea due to glucoamylase deficiency

disorder

SNOMED 716277000CUI C4275068

Overview

Chronic diarrhea due to glucoamylase deficiency 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

Abnormal small intestinal mucosa morphology

Frequent (30-79%)HP:0025129

Decreased small intestinal mucosa lactase level

Frequent (30-79%)HP:0025130

Dyspepsia

Frequent (30-79%)HP:0410281

Intestinal malabsorption

Frequent (30-79%)HP:0002024

Stomach pain

Frequent (30-79%)HP:0002027

Belly bloating

Occasional (5-29%)HP:0003270

Chronic diarrhoea

Occasional (5-29%)HP:0002028

Nausea

Occasional (5-29%)HP:0002018

Vomiting

Occasional (5-29%)HP:0002013

Related Conditions

Chronic diarrhea of infants AND/OR young children(parent)

Congenital disease(parent)

Gastrointestinal complication(parent)

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

Quick Facts

SNOMED CT: 716277000
UMLS CUI: C4275068
Fully Specified Name: Chronic diarrhea due to glucoamylase deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.