cerebral palsy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100021
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Genes

14 genes associated with the cerebral palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
ALAD aminolevulinate dehydratase
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
DNASE1L3 deoxyribonuclease I-like 3
HFE hemochromatosis
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
IDUA iduronidase, alpha-L-
SCN4A sodium channel, voltage gated, type IV alpha subunit
SLCO2A1 solute carrier organic anion transporter family, member 2A1
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
UROD uroporphyrinogen decarboxylase