Symphalangism Affecting The Phalanges Of The Hand Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Fusion of two or more phalangeal bones of the hand. (Human Phenotype Ontology, HP_0009773)
External Link https://www.disgenet.org/browser/0/1/0/C4021390
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Genes

13 genes associated with the disease Symphalangism Affecting The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BHLHA9 basic helix-loop-helix family, member a9
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
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
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