Search Ontology:
Human Disease

glycine encephalopathy 1

Term ID
DOID:0070616
Synonyms
  • GCE1
Definition
A glycine encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the GLDC gene, a member of the mitochondrial glycine cleavage system that encodes the P protein, on chromosome 9p24. (2)
References
Ontology
Human Disease   ( DOID:0070616 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models