MADD, MAP kinase activating death domain, 8567

N. diseases: 57; N. variants: 24
Disease: Deficiency of dehydrogenase ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1291311
Disease: Deficiency of dehydrogenase
Deficiency of dehydrogenase 		0.010 Biomarker disease BEFREE This review is focused on recent advances about GSDII and its treatment, and the most recent notions about the management and treatment of other metabolic myopathies will be briefly reviewed, including glycogenosis type V (McArdle disease), glycogenosis type III (debrancher enzyme deficiency or Cori disease), CPT-II deficiency, and ETF-dehydrogenase deficiency (also known as riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency or RR-MADD). 24997454 2015