Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome

disorder

SNOMED 1260140008CUI C5681444

Overview

Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Global developmental delay(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Genetic disease(parent)

Congenital cataract(parent)

Neonatal disease(parent)

Hepatic failure(parent)

Quick Facts

SNOMED CT: 1260140008
UMLS CUI: C5681444
Fully Specified Name: Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.