Polysyndactyly Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Polysyndactyly or PPD4 is a form of preaxial polydactyly of fingers (see this term), a limb malformation syndrome, characterized by the presence of a thumb showing the mildest degree of duplication, being broad, bifid or with radially deviated distal phalanx. Syndactyly of various degrees of third-and-fourth fingers is occasionally present. (Orphanet Rare Disease Ontology, Orphanet_93338)
External Link https://www.disgenet.org/browser/0/1/0/C0265553
Similar Terms
Downloads & Tools

Genes

11 genes associated with the disease Polysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BMP4 bone morphogenetic protein 4
CELSR2 cadherin, EGF LAG seven-pass G-type receptor 2
FAM92A1 family with sequence similarity 92, member A1
FZD4 frizzled class receptor 4
GLI3 GLI family zinc finger 3
HOXD13 homeobox D13
JAG2 jagged 2
LRP4 low density lipoprotein receptor-related protein 4
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
SMOC1 SPARC related modular calcium binding 1
WDPCP WD repeat containing planar cell polarity effector