Familial omphalocele syndrome with facial dysmorphism

disorder

SNOMED 770900000CUI C4749579

Overview

Familial omphalocele syndrome with facial dysmorphism is a disorder.

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

Related Conditions

Congenital anomaly of intestinal tract(parent)

Autosomal dominant hereditary disorder(parent)

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

Congenital omphalocele(parent)

Digestive system hereditary disorder(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 770900000
UMLS CUI: C4749579
Fully Specified Name: Familial omphalocele syndrome with facial dysmorphism (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.