Abnormality Of The Elbow Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An anomaly of the joint that connects the upper and the lower arm. (Human Phenotype Ontology, HP_0009811)
External Link https://www.disgenet.org/browser/0/1/0/C4021386
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Genes

12 genes associated with the disease Abnormality Of The Elbow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CCDC8 coiled-coil domain containing 8
CUL7 cullin 7
FGFR3 fibroblast growth factor receptor 3
GHR growth hormone receptor
GLE1 GLE1 RNA export mediator
IDUA iduronidase, alpha-L-
KLC4 kinesin light chain 4
KMT2A lysine (K)-specific methyltransferase 2A
OBSL1 obscurin-like 1
PPP1CB protein phosphatase 1, catalytic subunit, beta isozyme
SHOC2 soc-2 suppressor of clear homolog (C. elegans)
SMC1A structural maintenance of chromosomes 1A