| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Hand-foot-genital syndrome (HFGS) is a very rare multiple congenital abnormality syndrome characterized by distal limb malformations and urogenital defects. (Orphanet Rare Disease Ontology, Orphanet_2438) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C535627 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Hand foot uterus syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| HOXA13 | homeobox A13 | 2.88009 |
