Cholestasis-edema syndrome, Norwegian type

disorder

SNOMED 28724005CUI C0268314

Overview

Cholestasis-edema syndrome, Norwegian type is a disorder.

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

Clinical Trials

Total Trials

Recruiting

With Results

Recent Trials

Long-term Study of the DePuy Low Contact Stress (LCS) Complete Total Knee System

NCT00733915Phase 4Completed241 enrolled

View all 1 trials on ClinicalTrials.gov

Signs & Symptoms

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

Biliary tract disease

Very frequent (80-99%)HP:0001080

Discolored, acholic stools

Very frequent (80-99%)HP:0011985

Enlarged liver

Very frequent (80-99%)HP:0002240

Hyperlipidemia

Very frequent (80-99%)HP:0003077

Lymphatic disease

Very frequent (80-99%)HP:0100763

Lymphoedema

Very frequent (80-99%)HP:0001004

Nausea and vomiting

Very frequent (80-99%)HP:0002017

Neonatal cholestatic liver disease

Very frequent (80-99%)HP:0006566

Pee issues

Very frequent (80-99%)HP:0003110

Tiredness

Very frequent (80-99%)HP:0012378

Upset stomach

Very frequent (80-99%)HP:0002027

Yellowing of the skin

Very frequent (80-99%)HP:0000952

Abnormal skin colour

Frequent (30-79%)HP:0001000

Large spleen

Frequent (30-79%)HP:0001744

Lipomatosis

Frequent (30-79%)HP:0001012

Bone pain

Occasional (5-29%)HP:0002653

Cirrhosis

Occasional (5-29%)HP:0001394

Decreased bone mineral density Z score

Occasional (5-29%)HP:0004349

Gastrointestinal haemorrhage

Occasional (5-29%)HP:0002239

Portal hypertension

Occasional (5-29%)HP:0001409

Conjugated hyperbilirubinemia

HP:0002908

Elevated alkaline phosphatase

HP:0003155

Increased liver function tests

HP:0002910

Intestinal malabsorption

HP:0002024

St. Anthony's Fire

HP:0001055

Related Conditions

Digestive system hereditary disorder(parent)

Recessive hereditary disorder (autosomal)(parent)

Hereditary lymphedema(parent)

Cholestasis in newborn(parent)

Quick Facts

SNOMED CT: 28724005
UMLS CUI: C0268314
Fully Specified Name: Cholestasis-edema syndrome, Norwegian type (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 25
Clinical Trials: 1

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.