Mucocutaneous Lymph Node Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D009080
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Genes

4 genes/proteins associated with the disease Mucocutaneous Lymph Node Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ITPKC inositol-trisphosphate 3-kinase C 2.88009
BLK BLK proto-oncogene, Src family tyrosine kinase 2.88009
CD40 CD40 molecule, TNF receptor superfamily member 5 2.88009
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32) 2.88009