Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome

disorder

SNOMED 1172636006CUI C5567488

Overview

Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Chronic disease(parent)

Developmental hereditary disorder(parent)

Hereditary retinal dystrophy(parent)

Congenital coloboma of bilateral irides(parent)

Quick Facts

SNOMED CT: 1172636006
UMLS CUI: C5567488
Fully Specified Name: Familial progressive retinal dystrophy, iris coloboma, congenital cataract 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.