loading...| Preferred Name |
lattice corneal dystrophy |
| Synonyms |
familial amyloid neuropathy, Finnish type |
| Definitions |
An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and lattice line refractile and fleck-like opacification located_in the cornea, amyloid deposits beginning in the anterior stroma, and progressive vision loss later in life, and has_material_basis_in autosomal dominant inheritance of mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased amyloid protein deposition and disruption of the corneal surface. |
| ID |
http://purl.obolibrary.org/obo/DOID_8943 |
| database_cross_reference |
MESH:C537935 OMIM:122200 |
| has exact synonym |
familial amyloid neuropathy, Finnish type |
| id |
DOID:8943 |
| label |
lattice corneal dystrophy |
| notation |
DOID:8943 |
| prefLabel |
lattice corneal dystrophy |
| textual definition |
An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and lattice line refractile and fleck-like opacification located_in the cornea, amyloid deposits beginning in the anterior stroma, and progressive vision loss later in life, and has_material_basis_in autosomal dominant inheritance of mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased amyloid protein deposition and disruption of the corneal surface. |
| 引自 | |
| 有_obo_命名空间 |
disease_ontology |
| subClassOf |