Overview
Bilirubin-induced neurological dysfunction 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.
Abnormal auditory evoked potentials
Very frequent (80-99%)HP:0006958
Hepatic encephalopathy
Very frequent (80-99%)HP:0002480
Hyperbilirubinemia, neonatal
Very frequent (80-99%)HP:0003265
Jaundice, neonatal
Very frequent (80-99%)HP:0006579
Abnormal conjunctiva morphology
Frequent (30-79%)HP:0000502
Abnormal thalamic MRI signal intensity
Frequent (30-79%)HP:0012696
Central apnoea
Frequent (30-79%)HP:0002871
Conjunctival icterus
Frequent (30-79%)HP:0032106
CP
Frequent (30-79%)HP:0100021
Epilepsy
Frequent (30-79%)HP:0001250
Feeding difficulties
Frequent (30-79%)HP:0011968
Hemolytic anaemia
Frequent (30-79%)HP:0001878
Hypertonia
Frequent (30-79%)HP:0001276
Kernicterus
Frequent (30-79%)HP:0001343
Low albumin
Frequent (30-79%)HP:0003073
Mental deficiency
Frequent (30-79%)HP:0001249
Pyrexia
Frequent (30-79%)HP:0001945
Sensorineural deafness
Frequent (30-79%)HP:0000407
Hypernatremia
Occasional (5-29%)HP:0003228
Neonatal sepsis
Occasional (5-29%)HP:0040187
Visual gaze preference
Occasional (5-29%)HP:0025518
Quick Facts
- SNOMED CT
- 1197758001
- UMLS CUI
- C5575229
- Fully Specified Name
- Kernicterus spectrum disorder (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 21
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.