Mucocutaneous Lymph Node Syndrome Gene Set

Dataset	dbGAP Gene-Trait Associations
Category	disease or phenotype associations
Type	trait
Description	A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities. (Human Disease Ontology, DOID_13378)
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Genes

12 genes associated with the trait Mucocutaneous Lymph Node Syndrome in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Symbol	Name	Standardized Value
ADCK4	aarF domain containing kinase 4	1.0562
ITPKC	inositol-trisphosphate 3-kinase C	1.0562
FCGR2A	Fc fragment of IgG, low affinity IIa, receptor (CD32)	0.955241
MIA	melanoma inhibitory activity	0.897125
CENPU	centromere protein U	0.711358
TECRL	trans-2,3-enoyl-CoA reductase-like	0.585749
MED30	mediator complex subunit 30	0.552134
NAALADL2	N-acetylated alpha-linked acidic dipeptidase-like 2	0.50084
PELI1	pellino E3 ubiquitin protein ligase 1	0.443956
ZFHX3	zinc finger homeobox 3	0.443956
BTBD1	BTB (POZ) domain containing 1	0.323533
PPM1L	protein phosphatase, Mg2+/Mn2+ dependent, 1L	0.29992