Juvenile epithelial corneal dystrophy

disorder

SNOMED 1674008CUI C0339277

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Corneal dystrophy

HP:0001131

Decreased visual acuity

HP:0007663

Increased lacrimation

HP:0009926

Photophobia

HP:0000613

Punctate opacification of the cornea

HP:0007856

Related Conditions

Anterior corneal dystrophy(parent)

Hereditary corneal dystrophy(parent)

Corneal epithelial degeneration(parent)

Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT: 1674008
UMLS CUI: C0339277
Fully Specified Name: Juvenile epithelial corneal dystrophy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.