| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/140000 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the hand-foot-uterus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| HOXA13 | homeobox A13 |
