| Metadata | |
|---|---|
| ID | DOID:0080530 |
| Name | granular corneal dystrophy 1 |
| Definition | A granular corneal dystrophy that is characterized by recurrent erosions and gray crumb-like opacification located_in the cornea, proteinaceous rock candy-like deposits in the anterior stroma and subepithelium, and progressive vision loss later in life as deposits move into the central vision, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption of the corneal surface. https://pubmed.ncbi.nlm.nih.gov/8136834/ |
| Xrefs | |
| Synonyms |
corneal dystrophy, Groenouw type I [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |