Overview
Deficiency of isomaltase 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.
Diarrhea
Very frequent (80-99%)HP:0002014
Upset stomach
Very frequent (80-99%)HP:0002027
Dyschezia
Frequent (30-79%)HP:0002019
Flatulence
Frequent (30-79%)HP:0033589
Gastroesophageal reflux disease
Frequent (30-79%)HP:0002020
Nausea
Frequent (30-79%)HP:0002018
No appetite
Frequent (30-79%)HP:0004396
Vomiting
Frequent (30-79%)HP:0002013
Abdominal colic
Occasional (5-29%)HP:0011848
Abdominal swelling
Occasional (5-29%)HP:0003270
Anal incontinence
Occasional (5-29%)HP:0002607
Bloody stool
Occasional (5-29%)HP:0025085
Tiredness
Occasional (5-29%)HP:0012378
Postnatal failure to thrive
Very rare (1-4%)HP:0001508
Decreased mucosal sucrase-isomaltase activity
HP:0033597
Intestinal malabsorption
HP:0002024
Kidney stones
HP:0000787
Related Conditions
Quick Facts
- SNOMED CT
- 360854006
- UMLS CUI
- C1283620
- Fully Specified Name
- Deficiency of isomaltase (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
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.