|Name||corneal endothelial dystrophy 1 (autosomal dominant)|
|NCBI Gene ID||8197|
|Expression in Tissues and Cell Lines||
CHED1 has 28 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, functional term, phrase or reference) extracted from 3 datasets.
Click the + buttons to view associations for CHED1 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with CHED1 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|GeneRIF Biological Term Annotations||biological terms co-occuring with CHED1 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with CHED1 gene from the curated OMIM Gene-Disease Associations dataset.|