PFIC4 - progressive familial intrahepatic cholestasis type 4

disorder

SNOMED 1295517006CUI C2931067

Overview

PFIC4 - progressive familial intrahepatic cholestasis type 4 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

Hepatocellular carcinoma

Always present (100%)HP:0001402

Intrahepatic cholestasis

Always present (100%)HP:0001406

Hepatic insufficiency

Frequent (30-79%)HP:0001399

Portal hypertension

Occasional (5-29%)HP:0001409

Related Conditions

Progressive intrahepatic cholestasis(parent)

Quick Facts

SNOMED CT: 1295517006
UMLS CUI: C2931067
Fully Specified Name: Progressive familial intrahepatic cholestasis type 4 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.