inborn error of amino acid metabolism pathway
neurodevelopmental disorder pathway
AGAT deficiency pathway
2015-12-15T14:23:55Z
An autosomal recessive condition characterized by developmental delay and mental retardation due to defects in the GATM gene.
PW:0002359
SMP:00362
SMP:00507
VPetri
arginine:glycine amidinotransferase deficiency pathway
pathway