Adverse Drug Reaction Classification System

         

ADR Ontology
ADR Term Hyperglycinaemia
ADR ID BADD_A10063
ADR Hierarchy
03      Congenital, familial and genetic disorders
03.08      Metabolic and nutritional disorders congenital
03.08.04      Inborn errors of amino acid metabolism
03.08.04.011      Hyperglycinaemia
14      Metabolism and nutrition disorders
14.14      Inborn errors of metabolism
14.14.04      Inborn errors of amino acid metabolism
14.14.04.011      Hyperglycinaemia
17      Nervous system disorders
17.13      Encephalopathies
17.13.01      Encephalopathies toxic and metabolic
17.13.01.014      Hyperglycinaemia
18      Pregnancy, puerperium and perinatal conditions
18.04      Neonatal and perinatal conditions
18.04.04      Neonatal neurological system disorders NEC
18.04.04.016      Hyperglycinaemia
Description An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system. [MeSH]
MedDRA Code 10080883
MeSH ID D020158
ADR Severity Grade (FAERS) Not Available
ADR Severity Grade (CTCAE) Not Available
Synonym
Nonketotic hyperglycinaemia | Nonketotic hyperglycinemia | Hyperglycinaemia | Glycine encephalopathy | Hyperglycinemia | Hyperglycinemia, Nonketotic | Hyperglycinemias, Nonketotic | Nonketotic Hyperglycinemias | Nonketotic Hyperglycinemia | Glycine Encephalopathy | Encephalopathies, Glycine | Encephalopathy, Glycine | Glycine Encephalopathies | Non-ketotic Hyperglycinemia | Hyperglycinemia, Non-ketotic | Hyperglycinemias, Non-ketotic | Non ketotic Hyperglycinemia | Non-ketotic Hyperglycinemias | Hyperglycinemia, Nonketotic, Type III | Type III Nonketotic Hyperglycinemia | Nonketotic Hyperglycinemia, Type III | Hyperglycinemia, Nonketotic, Type I | Type I Nonketotic Hyperglycinemia | Nonketotic Hyperglycinemia, Type I | Hyperglycinemia, Nonketotic, Type II | Type II Nonketotic Hyperglycinemia | Nonketotic Hyperglycinemia, Type II
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D00696Divalproex sodium--
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