Overview
Macular 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.
Cloudy cornea
Very frequent (80-99%)HP:0007759
Corneal deposits
Very frequent (80-99%)HP:0000531
Laboratory abnormality
Very frequent (80-99%)HP:0001939
Punctate opacification of the cornea
Very frequent (80-99%)HP:0007856
Epithelial corneal erosions
Frequent (30-79%)HP:0000495
Severely impaired vision
Frequent (30-79%)HP:0001141
Thin cornea
Frequent (30-79%)HP:0100689
Decreased corneal sensitivity
Occasional (5-29%)HP:0012155
Eye pain
Occasional (5-29%)HP:0200026
Hyperopic astigmatism
Occasional (5-29%)HP:0000484
Photophobia
Occasional (5-29%)HP:0000613
Related Conditions
Congenital macular corneal dystrophy(child)
Macular corneal dystrophy Type I(child)
Macular corneal dystrophy Type II(child)
Spinocerebellar degeneration co-occurrent with macular corneal dystrophy(child)
Macular corneal dystrophy of bilateral corneas(child)
Stromal corneal dystrophy(parent)
Connective tissue hereditary disorder(parent)
Hereditary corneal dystrophy(parent)
Recessive hereditary disorder (autosomal)(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 60258001
- UMLS CUI
- C0024439
- Fully Specified Name
- Macular corneal dystrophy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 11
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.