increased urinary hypoxanthine Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased level of hypoxanthine in the urine. (Human Phenotype Ontology, HP_0011814)
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2 genes associated with the increased urinary hypoxanthine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MOCS1 molybdenum cofactor synthesis 1
MOCS2 molybdenum cofactor synthesis 2