|Name||Foveal hypoplasia and anterior segment dysgenesis|
|NCBI Gene ID||550626|
|Expression in Tissues and Cell Lines||
FHASD 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 FHASD from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with FHASD gene/protein from the curated CTD Gene-Disease Associations dataset.|