|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||disease cluster belonging to disease group unknown (Genetic Association Database)|
|Downloads & Tools|
1 genes associated with the disease amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
|MMACHC||methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria|