Syndromic orbital border hypoplasia

disorder

SNOMED 717337001CUI C4273912

Overview

Syndromic orbital border hypoplasia is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Congenital anomaly of orbit(parent)

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

Hereditary disorder of the visual system(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 717337001
UMLS CUI: C4273912
Fully Specified Name: Syndromic hypoplasia of orbital border (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.