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226 Possible Causes for Dimethylglycine Dehydrogenase Deficiency

  • Familial Hypercholesterolemia

    Dehydrogenase Deficiency 1 Disordered Steroidogenesis Due To Cytochrome P450 Oxidoreductase Deficiency 1 Distal Hereditary Motor Neuronopathy Type 2A 3 Distal Hereditary[preventiongenetics.com] 5 Dilated Cardiomyopathy 1S 7 Dilated Cardiomyopathy 1W 3 Dilated Cardiomyopathy 1X 4 Dilated Cardiomyopathy 1Y 6 Dilated Cardiomyopathy 1Z 1 Dilated Cardiomyopathy 2A 7 Dimethylglycine[preventiongenetics.com]

  • Generalized Epilepsy with Febrile Seizures Plus

    Glycine Encephalopathy Early Myoclonic Encephalopathy Show all 7 GLE1 GLE1 RNA export mediator 9q34.11 Lethal Congenital Contracture Syndrome 1, Lethal Arthrogryposis With[genecards.weizmann.ac.il] Glycine Encephalopathy, Neonatal Glycine Encephalopathy, Infantile Glycine Encephalopathy, Gcsh-Related Glycine Encephalopathy, Glycine Encephalopathy Desquamative Interstitial[genecards.weizmann.ac.il] Neoplasm GCSAM germinal center-associated, signaling and motility 3q13.2 Diffuse Large B-Cell Lymphoma GCSH glycine cleavage system protein H (aminomethyl carrier) 16q23.2 Atypical[genecards.weizmann.ac.il]

  • Dilated Cardiomyopathy Type 2B

    Dehydrogenase Deficiency 1 Disordered Steroidogenesis Due To Cytochrome P450 Oxidoreductase Deficiency 1 Distal Hereditary Motor Neuronopathy Type 2A 3 Distal Hereditary[preventiongenetics.com] 5 Dilated Cardiomyopathy 1S 7 Dilated Cardiomyopathy 1W 3 Dilated Cardiomyopathy 1X 4 Dilated Cardiomyopathy 1Y 6 Dilated Cardiomyopathy 1Z 1 Dilated Cardiomyopathy 2A 7 Dimethylglycine[preventiongenetics.com]

  • Familial Recurrent Peripheral Facial Palsy

    glycine encephalopathy Atypical juvenile parkinsonism Atypical pantothenate kinase-associated neurodegeneration Atypical progressive supranuclear palsy syndrome Autism spectrum[se-atlas.de] […] syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Atkin-Flaitz syndrome Attenuated Chédiak-Higashi syndrome Atypical Rett syndrome Atypical autism Atypical[se-atlas.de]

  • Biotin-Responsive Basal Ganglia Disease

    Dimethylglycine dehydrogenase deficiency Disorder of O-N-acetylgalactosaminylglycan synthesis Disorder of O-mannosylglycan synthesis Disorder of O-xylosyl/N-acetylgalactosaminylglycan[se-atlas.de] deficiency Dicarboxylic aminoaciduria Dihydropteridine reductase deficiency Dihydropyrimidine dehydrogenase deficiency Dihydropyrimidinuria Dilated cardiomyopathy with ataxia[se-atlas.de] glycine encephalopathy Atypical hypotonia-cystinuria syndrome Atypical pantothenate kinase-associated neurodegeneration Autism spectrum disorder-epilepsy-arthrogryposis syndrome[se-atlas.de]

  • Halitosis

    Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency. Am J Hum Genet 2001; 68 : 839–847. 97.[doi.org]

  • Hereditary Hyperekplexia

    […] type, with taurodontism) DMD (Becker muscular dystrophy) DMGDH (Dimethylglycine dehydrogenase deficiency) DMP1 (Hypophosphatemic rickets, AR) DMPK (Myotonic dystrophy) DNAH11[en.praenatal-medizin.de] E2 deficiency) DLD (Leigh syndrome) DLEC1 (Esophageal cancer) DLL3 (Spondylocostal dysostosis, autosomal recessive, 1) DLX3 (Amelogenesis imperfecta, hypomaturation-hypoplastic[en.praenatal-medizin.de] FRA12A type) DIRC2 (Renal cell carcinoma) DISC2 (Schizophrenia) DJ1 (Parkinson disease 7, autosomal recessive early-onset) DKC1 (Dyskeratosis congenita-1) DLAT (Pyruvate dehydrogenase[en.praenatal-medizin.de]

  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    glycine encephalopathy Atypical juvenile parkinsonism Atypical pantothenate kinase-associated neurodegeneration Atypical progressive supranuclear palsy syndrome Autism spectrum[se-atlas.de] […] syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Atkin-Flaitz syndrome Attenuated Chédiak-Higashi syndrome Atypical Rett syndrome Atypical autism Atypical[se-atlas.de]

  • Distal Hereditary Motor Neuropathy Type 1

    glycine encephalopathy Atypical juvenile parkinsonism Atypical pantothenate kinase-associated neurodegeneration Atypical progressive supranuclear palsy syndrome Autism spectrum[se-atlas.de] […] syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Atkin-Flaitz syndrome Attenuated Chédiak-Higashi syndrome Atypical Rett syndrome Atypical autism Atypical[se-atlas.de]

  • 2-Aminoadipic 2-Oxoadipic Aciduria

    Diaminopentanuria Dibasic Amino Aciduria I dicarboxylic aminoaciduria Dimethylglycine Dehydrogenase Deficiency GABA aminotransferase deficiency gamma-amino butyric acid metabolism[rgd.mcw.edu] deficiency Dihydropyrimidinuria Dimethylglycine dehydrogenase deficiency Dyggve-Melchior-Clausen disease Efavirenz, poor metabolism of Enterokinase deficiency Erythrocyte[qlinics.com] […] kinase deficiency Brunner syndrome Camptodactyly Taurinuria Carboxypeptidase N Deficiency cerebral creatine deficiency syndrome cystathioninuria Cysteine Peptiduria cystinuria[rgd.mcw.edu]

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