| Metadata | |
|---|---|
| ID | DOID:0060455 |
| Name | Thiel-Behnke corneal dystrophy |
| Definition | An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and honeycomb-shaped opacification located_in the cornea, proteinaceous deposits in the anterior stroma and subepithelium, and progressive early vision loss, 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 especially of Bowman's membrane of the cornea. https://www.omim.org/entry/602082 |
| Xrefs |
SNOMEDCT_US_2023_03_01:417065002 |
| Subsets |
DO_rare_slim |
| Synonyms |
anterior limiting membrane dystrophy type II [EXACT] corneal dystrophy honeycomb-shaped [EXACT] corneal dystrophy of Bowman layer type II [EXACT] TBCD [EXACT] Waardenburg-Jonker corneal dystrophy [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |