Child Nutrition Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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6 genes associated with the Child Nutrition Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CAT catalase
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CYBA cytochrome b-245, alpha polypeptide
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
NQO1 NAD(P)H dehydrogenase, quinone 1
SOD2 superoxide dismutase 2, mitochondrial