Progressive familial intrahepatic cholestasis type 3

disorder

SNOMED 1186865008CUI C1865643

Overview

Progressive familial intrahepatic cholestasis type 3 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.

Cirrhosis

Always present (100%)HP:0001394

Diarrhea

Always present (100%)HP:0002014

Elevated gamma-glutamyltransferase level

Always present (100%)HP:0030948

Enlarged liver

Always present (100%)HP:0002240

Large spleen

Always present (100%)HP:0001744

Portal fibrosis shown on biopsy

Always present (100%)HP:0006580

Skin itching

Always present (100%)HP:0000989

Subclinical abnormal liver function tests

Always present (100%)HP:0002910

Yellowing of the skin

Always present (100%)HP:0000952

Ascites

Frequent (30-79%)HP:0001541

Increased serum bile acid concentration

Frequent (30-79%)HP:0012202

Portal inflammation

Frequent (30-79%)HP:0033196

Proliferation of bile canaliculi

Frequent (30-79%)HP:0001408

Intestinal malabsorption

HP:0002024

Intrahepatic cholestasis

HP:0001406

Related Conditions

Progressive intrahepatic cholestasis(parent)

Quick Facts

SNOMED CT: 1186865008
UMLS CUI: C1865643
Fully Specified Name: Progressive familial intrahepatic cholestasis type 3 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.