Overview
Groenouw corneal dystrophy type I 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.
Central corneal dystrophy
Very frequent (80-99%)HP:0007881
Corneal deposits
Very frequent (80-99%)HP:0000531
Central opacification of the cornea
Frequent (30-79%)HP:0011493
Epithelial corneal erosions
Frequent (30-79%)HP:0000495
Poor vision
Frequent (30-79%)HP:0000505
Abnormal corneal epithelium morphology
Occasional (5-29%)HP:0011495
Decreased visual acuity
Occasional (5-29%)HP:0007663
Eye pain
Occasional (5-29%)HP:0200026
Photophobia
Occasional (5-29%)HP:0000613
Subepithelial corneal opacities
Occasional (5-29%)HP:0008039
Granular corneal dystrophy
HP:0007802
Lens opacities
HP:0000518
Nodular corneal dystrophy
HP:0007827
Punctate corneal dystrophy
HP:0007809
Squint
HP:0000486
Related Conditions
Quick Facts
- SNOMED CT
- 419039007
- UMLS CUI
- C1641846
- Fully Specified Name
- Granular corneal dystrophy type I (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 15
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.