Visualize Submit Comment

Metadata
ID	DOID:0061001
Name	glycine encephalopathy 2
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. https://pubmed.ncbi.nlm.nih.gov/8005589/
Xrefs	MIM:620398
Synonyms	GCE2 [EXACT]
Parent Relationships	is_a glycine encephalopathy