Term Name:	glycine encephalopathy 2
Synonyms:	GCE2
Definition:	A glycine encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the AMT gene, which encodes a member of the glycine cleavage system (protein T), on chromosome 3p21.
Ontology:	Human Disease [DOID:0061001]   ( DOID:0061001 )