Hepatoportal sclerosis

disorder

SNOMED 718096004CUI C4273756

Overview

Hepatoportal sclerosis 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.

Large spleen

Very frequent (80-99%)HP:0001744

Low number of red blood cells or haemoglobin

Very frequent (80-99%)HP:0001903

Abnormal liver parenchyma morphology

Frequent (30-79%)HP:0030146

Abnormality of liver blood vessels

Frequent (30-79%)HP:0006707

Bleeding tendency

Frequent (30-79%)HP:0001892

Esophageal varix

Frequent (30-79%)HP:0002040

Gastric varix

Frequent (30-79%)HP:0030169

Hypersplenism

Frequent (30-79%)HP:0001971

Incomplete septal cirrhosis

Frequent (30-79%)HP:0031015

Leukopenia

Frequent (30-79%)HP:0001882

Low factor II activity

Frequent (30-79%)HP:0008151

Portal hypertension

Frequent (30-79%)HP:0001409

Smooth muscle antibody positive

Frequent (30-79%)HP:0003262

Abnormal liver enzymes

Occasional (5-29%)HP:0002910

Anticardiolipin IgG antibody positivity

Occasional (5-29%)HP:0020136

Anticardiolipin IgM antibody positivity

Occasional (5-29%)HP:0020137

Ascites

Occasional (5-29%)HP:0001541

Cognitive deficits

Occasional (5-29%)HP:0100543

Gastrointestinal haemorrhage

Occasional (5-29%)HP:0002239

Hepatic encephalopathy

Occasional (5-29%)HP:0002480

High blood bilirubin levels

Occasional (5-29%)HP:0002904

Low albumin

Occasional (5-29%)HP:0003073

Low platelet count

Occasional (5-29%)HP:0001873

Partial nodular transformation of liver

Occasional (5-29%)HP:0011954

Periportal fibrosis

Occasional (5-29%)HP:0001405

Portal vein thrombosis

Occasional (5-29%)HP:0030242

Predisposition to infections

Occasional (5-29%)HP:0002719

Skin itching

Occasional (5-29%)HP:0000989

Yellowing of the skin

Occasional (5-29%)HP:0000952

Increased incidence of hepatocellular carcinoma

Very rare (1-4%)HP:0001402

Related Conditions

Disorder of hepatic portal vein(parent)

Vascular degeneration(parent)

PSVD - porto sinusoidal vascular disease(parent)

Quick Facts

SNOMED CT: 718096004
UMLS CUI: C4273756
Fully Specified Name: Hepatoportal sclerosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.