FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term glycine encephalopathy 1 ID (Ontology) DOID:0070616 (Human Disease)
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.
Also Known As "GCE1"
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 Genes
 glycine encephalopathy 1       1
 for disease ribbon | glycine encephalopathy 1       1
 model of | glycine encephalopathy 1       1
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autosomal recessive disease____
amino acid metabolic disorder__|
                               glycine encephalopathy
                                |__glycine encephalopathy 1  1 rec.
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Is a glycine encephalopathy
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Synonyms
  • "GCE1" EXACT OMO:0003012
Secondary IDs
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MIM:605899