Overview
By MedlinePlus, National Library of Medicine
NIH: National Eye Institute Courtesy of the National Library of Medicine. Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal corneal endothelium morphology
Very frequent (80-99%)HP:0011488
Abnormality of Descemet's membrane
Very frequent (80-99%)HP:0011490
Corneal opacity
Very frequent (80-99%)HP:0007957
Decreased visual acuity
Very frequent (80-99%)HP:0007663
Reduced number of corneal endothelial cells
Very frequent (80-99%)HP:0011491
Water retention
Very frequent (80-99%)HP:0000969
Eye movement-induced pain
Frequent (30-79%)HP:0030857
Night blindness
Frequent (30-79%)HP:0000662
Visual loss
Frequent (30-79%)HP:0000572
Related Conditions
Quick Facts
- SNOMED CT
- 193839007
- UMLS CUI
- C0016781
- Fully Specified Name
- Fuchs' corneal dystrophy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 9
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.