|Name||Myopia 20, autosomal dominant|
|NCBI Gene ID||100682326|
|Expression in Tissues and Cell Lines||
MYP20 has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for MYP20 from the datasets below.
If available, associations are ranked by standardized value
|OMIM Gene-Disease Associations||phenotypes associated with MYP20 gene from the curated OMIM Gene-Disease Associations dataset.|