preaxial foot polydactyly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Duplication of all or part of the first ray. (Human Phenotype Ontology, HP_0001841)
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23 genes associated with the preaxial foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
BMP2 bone morphogenetic protein 2
EFNB1 ephrin-B1
FGF10 fibroblast growth factor 10
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLNA filamin A, alpha
GATA4 GATA binding protein 4
GLI3 GLI family zinc finger 3
HOXD13 homeobox D13
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8
KIF7 kinesin family member 7
LMBR1 limb development membrane protein 1
MIPOL1 mirror-image polydactyly 1
NEK1 NIMA-related kinase 1
RAB23 RAB23, member RAS oncogene family
ROR2 receptor tyrosine kinase-like orphan receptor 2
SALL1 spalt-like transcription factor 1
SALL4 spalt-like transcription factor 4
SATB2 SATB homeobox 2
SHH sonic hedgehog
SUMF1 sulfatase modifying factor 1