cerebral palsy; Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A brain disease that is caused by damage to the motor control centers of the developing brain during pregnancy, during childbirth or after birth, which affects muscle movement and balance. (Human Disease Ontology, DOID_1969)
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Genes

21 genes associated with the disease cerebral palsy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADD1 adducin 1 (alpha)
ADRB2 adrenoceptor beta 2, surface
ALOX5AP arachidonate 5-lipoxygenase-activating protein
ANXA5 annexin A5
CBS cystathionine-beta-synthase
CXCL8 chemokine (C-X-C motif) ligand 8
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
F7 coagulation factor VII (serum prothrombin conversion accelerator)
FGB fibrinogen beta chain
LTA lymphotoxin alpha
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS2 nitric oxide synthase 2, inducible
NOS3 nitric oxide synthase 3 (endothelial cell)
PDE4D phosphodiesterase 4D, cAMP-specific
PLAT plasminogen activator, tissue
PROCR protein C receptor, endothelial
SERPINB2 serpin peptidase inhibitor, clade B (ovalbumin), member 2
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
TFPI tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)
THBD thrombomodulin