Gershoni Baruch syndrome

disorder

SNOMED 1172589000CUI C1836007

Overview

Gershoni Baruch syndrome is a disorder.

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

Related Conditions

Congenital omphalocele(parent)

Multiple malformation syndrome with facial-limb defects as major feature(parent)

Genetic disease(parent)

Quick Facts

SNOMED CT: 1172589000
UMLS CUI: C1836007
Fully Specified Name: Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect 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.