|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Lack of urothione (the urinary metabolite of molybdenum cofactor) in the urine. (Human Phenotype Ontology, HP_0003606)|
|Downloads & Tools|
1 genes associated with the absent urinary urothione phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|MOCS1||molybdenum cofactor synthesis 1|