Gelatinous droplike corneal dystrophy

disorder

SNOMED 419900000CUI C0339273

Overview

Gelatinous droplike corneal dystrophy is a disorder.

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

Signs & Symptoms

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

Blurred vision

Very frequent (80-99%)HP:0000622

Photophobia

Very frequent (80-99%)HP:0000613

Conjunctival amyloidosis

Frequent (30-79%)HP:0010637

Conjunctival foreign body sensation

Frequent (30-79%)HP:0034804

Corneal vascularization

Frequent (30-79%)HP:0011496

Decreased visual acuity

Frequent (30-79%)HP:0007663

Eye pain

Frequent (30-79%)HP:0200026

Increased lacrimation

Frequent (30-79%)HP:0009926

Involuntary closure of eyelid

Frequent (30-79%)HP:0000643

Subepithelial corneal opacities

Frequent (30-79%)HP:0008039

Central opacification of the cornea

Occasional (5-29%)HP:0011493

Corneal dystrophy

HP:0001131

Poor vision

HP:0000505

Related Conditions

Corneal deposit(parent)

Stromal corneal dystrophy(parent)

Connective tissue hereditary disorder(parent)

Recessive hereditary disorder (autosomal)(parent)

Hereditary corneal dystrophy(parent)

Ocular amyloid deposit(parent)

Hereditary amyloidosis(parent)

Quick Facts

SNOMED CT: 419900000
UMLS CUI: C0339273
Fully Specified Name: Gelatinous droplike corneal dystrophy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.