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MIRAGE
congenital stromal corneal dystrophy
Summary
- Synonym
-
- CSCD
- congenital hereditary stromal dystrophy
- Definition
- A stromal dystrophy that is characterized by the presence of bilateral corneal opacities that can be seen at or shortly after birth.
- Super Class
- physical disorder stromal dystrophy
External Links
- Disease Ontology
- DOID:0060445
- Mondo Disease Ontology
- MeSH
- ORDO
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000529 | Progressive visual loss |
| HP:0007709 | Band-shaped corneal dystrophy |
| HP:0000486 | Strabismus |
| HP:0200020 | Corneal erosion |
| HP:0001131 | Corneal dystrophy |
| HP:0000006 | Autosomal dominant inheritance |
| HP:0003623 | Neonatal onset |
| HP:0000501 | Glaucoma |
| HP:0011487 | Increased corneal thickness |
| HP:0000613 | Photophobia |
