Congenital secretory diarrhea, chloride type

disorder

SNOMED 24412005CUI C0267662

Overview

Congenital secretory diarrhea, chloride type 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.

Elevated serum bicarbonate concentration

Always present (100%)HP:0032067

Elevations in faecal chloride concentration

Always present (100%)HP:0034470

Hyperaldosteronism

Always present (100%)HP:0000859

Increased plasma renin

Always present (100%)HP:0000848

Low blood potassium levels

Always present (100%)HP:0002900

Secretory diarrhea

Always present (100%)HP:0005208

Abdominal swelling

HP:0003270

Alkalosis

HP:0001948

Dehydration

HP:0001944

Growth abnormality

HP:0001507

Growth failure

HP:0001510

Hydramnios

HP:0001561

Hyponatremia

HP:0002902

Increased plasma renin activity

HP:0000841

Low blood chloride levels

HP:0003113

Metabolic alkalosis

HP:0200114

Premature birth

HP:0001622

Undergrowth

HP:0001508

Related Conditions

Congenital secretory diarrhea(parent)

Malabsorption syndrome(parent)

Digestive system hereditary disorder(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 24412005
UMLS CUI: C0267662
Fully Specified Name: Congenital secretory diarrhea, chloride type (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 18

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.