Definition: An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system.
Do not confuse with HYPERGLYCEMIC HYPEROSMOLAR NONKETOTIC COMA
Other names Nonketotic Hyperglycinemias; Non-ketotic Hyperglycinemias; Non ketotic Hyperglycinemia; Hyperglycinemias, Nonketotic; Hyperglycinemias, Non-ketotic; Hyperglycinemia, Non-ketotic; Glycine Encephalopathies; Encephalopathy, Glycine; Encephalopathies, Glycine; Type III Nonketotic Hyperglycinemia; Type II Nonketotic Hyperglycinemia; Type I Nonketotic Hyperglycinemia; Nonketotic Hyperglycinemia, Type III; Nonketotic Hyperglycinemia, Type II; Nonketotic Hyperglycinemia, Type I; Non-ketotic Hyperglycinemia; Hyperglycinemia, Nonketotic, Type III; Hyperglycinemia, Nonketotic, Type II; Hyperglycinemia, Nonketotic, Type I; Glycine Encephalopathy
