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