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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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