absent urinary urothione Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of urothione (the urinary metabolite of molybdenum cofactor) in the urine. (Human Phenotype Ontology, HP_0003606)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003606
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Genes

1 genes associated with the absent urinary urothione phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MOCS1 molybdenum cofactor synthesis 1