Search Ontology:
Human Disease

glycine encephalopathy 2

Term ID
DOID:0061001
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. https://pubmed.ncbi.nlm.nih.gov/8005589/
References
Ontology
Human Disease   ( DOID:0061001 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
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