Hand foot uterus syndrome Gene Set

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
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Genes

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