amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group unknown (Genetic Association Database)
Similar Terms
Downloads & Tools

Genes

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.

Symbol Name
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria