| H01003 | |
| H number | H01003 |
| Name | Dimethylglycine dehydrogenase deficiency |
| Description | Dimethylglycine dehydrogenase deficiency (DMGDHD) is a rare autosomal recessive disorder characterized by fish odor, and unusual muscle fatigue with increased serum creatine kinase. Dimethylglycine dehydrogenase (DMGDH) is a mitochondrial matrix enzyme involved in the metabolism of choline. |
| Category | Inherited metabolic disorder |
| Network | - |
| Gene | (DMGDHD) DMGDH [HSA:29958] [KO:K00315] |
| Pathogen | - |
| Env factor | - |
| Carcinogen | - |
| Drug | - |
| Comment | - |
| Other DBs | ICD-11: 5C50.7 ICD-10: E72.5 MeSH: C565278 OMIM: 605850 268900 |
| Reference | PMID:11231903 AUTHORS Binzak BA, Wevers RA, Moolenaar SH, Lee YM, Hwu WL, Poggi-Bach J, Engelke UF, Hoard HM, Vockley JG, Vockley J TITLE Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency. JOURNAL Am J Hum Genet 68:839-47 (2001) DOI:10.1086/319520 |