Ablepharon

disorder

SNOMED 13401001CUI C0266574

Overview

Ablepharon is a disorder.

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

Related Conditions

Partial ablepharon(child)

Congenital absence of eyelid(child)

Ablepharon macrostomia syndrome(child)

Ablepharon of bilateral eyelids(child)

Congenital anomaly of eyelid(parent)

Quick Facts

SNOMED CT: 13401001
UMLS CUI: C0266574
Fully Specified Name: Ablepharon (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.