Opsoclonus-Myoclonus Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Opsoclonus myoclonus syndrome (OMS) is a rare pediatric brain inflammatory disease of paraneoplastic, parainfectious or idiopathic origin, characterized by opsoclonus, myoclonus, ataxia and behavioural and sleep disorders. (Orphanet Rare Disease Ontology, Orphanet_1183)
External Link	https://www.disgenet.org/browser/0/1/0/C0393626
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Genes

14 genes associated with the disease Opsoclonus-Myoclonus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
CCL17	chemokine (C-C motif) ligand 17
CCL22	chemokine (C-C motif) ligand 22
CCR4	chemokine (C-C motif) receptor 4
CSF2	colony stimulating factor 2 (granulocyte-macrophage)
GPI	glucose-6-phosphate isomerase
IGF1	insulin-like growth factor 1 (somatomedin C)
KCTD7	potassium channel tetramerization domain containing 7
LAMC2	laminin, gamma 2
MYCN	v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
PIK3CA	phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PIK3CB	phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
PIK3CD	phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
PIK3CG	phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
POMC	proopiomelanocortin