symphalangism affecting the phalanges of the hand Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Fusion of two or more phalangeal bones of the hand. (Human Phenotype Ontology, HP_0009773)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009773
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Genes

15 genes associated with the symphalangism affecting the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMPR1B bone morphogenetic protein receptor, type IB
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
FGF9 fibroblast growth factor 9
FGFR2 fibroblast growth factor receptor 2
GDF5 growth differentiation factor 5
HOXD13 homeobox D13
IHH indian hedgehog
MYH8 myosin, heavy chain 8, skeletal muscle, perinatal
NOG noggin
PTDSS1 phosphatidylserine synthase 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
SLC26A2 solute carrier family 26 (anion exchanger), member 2
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
TPM2 tropomyosin 2 (beta)
WNT7A wingless-type MMTV integration site family, member 7A