Overview
Avellino 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.
Lattice corneal dystrophy
Always present (100%)HP:0001149
Central opacification of the cornea
Very frequent (80-99%)HP:0011493
Corneal deposits
Very frequent (80-99%)HP:0000531
Granular corneal dystrophy
Very frequent (80-99%)HP:0007802
Corneal stromal opacity
Frequent (30-79%)HP:0007759
Decreased visual acuity
Frequent (30-79%)HP:0007663
Poor vision
Frequent (30-79%)HP:0000505
Subepithelial corneal opacities
Frequent (30-79%)HP:0008039
Blurred vision
Occasional (5-29%)HP:0000622
Recurrent breakdown of clear protective layer of eye
Occasional (5-29%)HP:0000495
Related Conditions
Quick Facts
- SNOMED CT
- 397568004
- UMLS CUI
- C1275685
- Fully Specified Name
- Granular corneal dystrophy type II (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 10
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.