Crigler-Najjar syndrome, type II

disorder

SNOMED 68067009CUI C2931132

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Yellowing of the skin

Always present (100%)HP:0000952

Hyperbilirubinemia, neonatal

Very frequent (80-99%)HP:0003265

Prolonged neonatal jaundice

Very frequent (80-99%)HP:0006579

Unconjugated hyperbilirubinemia

Very frequent (80-99%)HP:0008282

Abnormal liver function

Excluded (<1%)HP:0002910

Reduced tissue uridine diphosphate glucuronosyltransferase activity

HP:6000617

Related Conditions

Crigler-Najjar syndrome(parent)

Quick Facts

SNOMED CT: 68067009
UMLS CUI: C2931132
Fully Specified Name: Crigler-Najjar syndrome, type II (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.