hand-foot-uterus syndrome Gene Set

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
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Genes

1 genes associated with the hand-foot-uterus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
HOXA13 homeobox A13