Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormality of the cornea
Very frequent (80-99%)HP:0000481
Central opacification of the cornea
Very frequent (80-99%)HP:0011493
Corneal scarring
Very frequent (80-99%)HP:0000559
Lattice corneal dystrophy
Very frequent (80-99%)HP:0001149
Scarring or clouding of the cornea of the eye
Very frequent (80-99%)HP:0007957
Visual loss
Very frequent (80-99%)HP:0000572
Abnormal curving of the cornea or lens of the eye
Frequent (30-79%)HP:0000483
Corneal stromal edema
Frequent (30-79%)HP:0012040
Epithelial corneal erosions
Frequent (30-79%)HP:0000495
Eye pain
Frequent (30-79%)HP:0200026
Photophobia
Frequent (30-79%)HP:0000613
Red eyes
Frequent (30-79%)HP:0025337
Subepithelial corneal opacities
Frequent (30-79%)HP:0008039
Central posterior corneal opacity
Occasional (5-29%)HP:0008511
Corneal hypesthesia
Occasional (5-29%)HP:0012155
Decreased visual acuity, slowly progressive
Occasional (5-29%)HP:0007924
Severe myopia
Occasional (5-29%)HP:0011003
Progressive visual loss
HP:0000529
Related Conditions
Quick Facts
- SNOMED CT
- 419197009
- UMLS CUI
- C1690006
- Fully Specified Name
- Lattice corneal dystrophy Type I (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 18
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.