Carpal Synostosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Synostosis (bony fusion) involving one or more bones of the carpus (scaphoid, lunate, triquetrum, trapezium, trapezoid, capitate, hamate, pisiform). (Human Phenotype Ontology, HP_0009702)
External Link https://www.disgenet.org/browser/0/1/0/C0431863
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Genes

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

Symbol Name
BMPR1B bone morphogenetic protein receptor, type IB
CHSY1 chondroitin sulfate synthase 1
FBLN1 fibulin 1
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
GDF5 growth differentiation factor 5
HOXD13 homeobox D13
MAP3K7 mitogen-activated protein kinase kinase kinase 7
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NOG noggin
PAX3 paired box 3
POR P450 (cytochrome) oxidoreductase
RBM8A RNA binding motif protein 8A
RECQL4 RecQ protein-like 4
SALL4 spalt-like transcription factor 4