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.

Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome — Symptoms, Testing & Specialists | Ltrl