Indian childhood cirrhosis

disorder

SNOMED 6183001CUI C0268074

Overview

Indian childhood cirrhosis 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.

Esophageal varix

Always present (100%)HP:0002040

Peritoneal effusion

Always present (100%)HP:0001541

Cirrhosis

Frequent (30-79%)HP:0001394

Biliary cirrhosis

Occasional (5-29%)HP:0002613

Fulminant hepatitis

Occasional (5-29%)HP:0004787

Abdominal swelling

HP:0003270

High blood pressure

HP:0000822

Increased level of L-fucose in urine

HP:0410067

Increased level of propane-1,2-diol in blood

HP:0410069

Languor

HP:0001254

Micronodular cirrhosis

HP:0001413

Primary pulmonary hypertension

HP:0002092

Pyrexia

HP:0001945

Yellowing of the skin

HP:0000952

Related Conditions

Cirrhosis of liver(parent)

Disorder of copper metabolism(parent)

Chronic metabolic disease(parent)

Quick Facts

SNOMED CT: 6183001
UMLS CUI: C0268074
Fully Specified Name: Indian childhood cirrhosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.