1.5.5.1 Acidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8617498&form=6&db=m Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human. causal interaction,ongoing research,therapeutic application,unassigned 4,1,1,0 1.5.5.1 Acidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17912479&form=6&db=m Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 Acidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17977044&form=6&db=m Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II. unassigned - 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7360517&form=6&db=m Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein. causal interaction,unassigned 3,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9889013&form=6&db=m Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism. causal interaction,diagnostic usage,unassigned 1,3,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16165386&form=6&db=m Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiency. causal interaction,ongoing research,unassigned 2,2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16510302&form=6&db=m Electron transfer flavoprotein deficiency: functional and molecular aspects. causal interaction,diagnostic usage,therapeutic application,unassigned 4,2,1,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17050691&form=6&db=m Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool. causal interaction,ongoing research,unassigned 1,2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17912479&form=6&db=m Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19249206&form=6&db=m ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,unassigned 2,2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19265687&form=6&db=m Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 3,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19774399&form=6&db=m Characterizing the transcriptional regulation of let-721, a Caenorhabditis elegans homolog of human electron flavoprotein dehydrogenase. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20138856&form=6&db=m High resolution melting analysis facilitates mutation screening of ETFDH gene: applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20392676&form=6&db=m In vitro probe acylcarnitine profiling assay using cultured fibroblasts and electrospray ionization tandem mass spectrometry predicts severity of patients with glutaric aciduria type 2. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20674745&form=6&db=m Mutational hotspots in electron transfer flavoprotein underlie defective folding and function in multiple acyl-CoA dehydrogenase deficiency. unassigned - 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20937244&form=6&db=m The electron transfer flavoprotein: Ubiquinone oxidoreductases. unassigned - 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21596162&form=6&db=m Characterization of mitochondrial proteome in a severe case of ETF-QO deficiency. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22190129&form=6&db=m Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect. causal interaction,unassigned 2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23106979&form=6&db=m A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene. causal interaction,unassigned 2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24357026&form=6&db=m Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,unassigned 3,3,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25200064&form=6&db=m Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency. causal interaction,unassigned 3,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25913573&form=6&db=m A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency (MADD) with a novel mutation in ETFDH gene. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27000805&form=6&db=m Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,therapeutic application,unassigned 3,2,1,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28914566&form=6&db=m A novel ETFDH mutation in an adult patient with late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29249369&form=6&db=m A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29615056&form=6&db=m Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report. causal interaction,therapeutic application,unassigned 4,1,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29988809&form=6&db=m Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30003820&form=6&db=m Coenzyme Q10 serves to couple mitochondrial oxidative phosphorylation and fatty acid ?-oxidation, and attenuates NLRP3 inflammasome activation. unassigned - 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30022752&form=6&db=m [A novel mutation in the ETFDH gene of an infant with multiple acyl-CoA dehydrogenase deficiency]. causal interaction,diagnostic usage,unassigned 4,4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30027710&form=6&db=m Clinical Features of Multiple Acyl-CoA Dehydrogenase Deficiency With ETFDH Variants in the First Korean Cases. diagnostic usage,unassigned 3,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30424791&form=6&db=m Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30508893&form=6&db=m Long-term outcomes of a patient with late-onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutations in ETFDH: A case report. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30709034&form=6&db=m ETF-QO Mutants Uncoupled Fatty Acid ?-Oxidation and Mitochondrial Bioenergetics Leading to Lipid Pathology. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30982706&form=6&db=m Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report. causal interaction,unassigned 2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31058673&form=6&db=m Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31392824&form=6&db=m FLAD1-associated multiple acyl-CoA dehydrogenase deficiency identified by newborn screening. causal interaction,diagnostic usage,unassigned 4,3,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31852447&form=6&db=m Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations. causal interaction,therapeutic application,unassigned 3,1,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31997039&form=6&db=m Multiple acyl-COA dehydrogenase deficiency in elderly carriers. ongoing research,unassigned 2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32064983&form=6&db=m Skin damage in a patient with lipid storage myopathy with a novel ETFDH mutation responsive to riboflavin. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32292771&form=6&db=m A Synonymous Variant c.579A>G in the ETFDH Gene Caused Exon Skipping in a Patient With Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Case Report. causal interaction,unassigned 2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32393189&form=6&db=m A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32499892&form=6&db=m Correlation between ETFDH mutations and dysregulation of serum myomiRs in MADD patients. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32925727&form=6&db=m Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: A case report and a literature review. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33131365&form=6&db=m A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33438237&form=6&db=m CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,therapeutic application,unassigned 3,1,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33720849&form=6&db=m Targeted Therapies for Metabolic Myopathies Related to Glycogen Storage and Lipid Metabolism: a Systematic Review and Steps Towards a 'Treatabolome'. unassigned - 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33732619&form=6&db=m Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screening. unassigned - 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33823724&form=6&db=m ETF dehydrogenase advances in molecular genetics and impact on treatment. causal interaction,unassigned 4,0 1.5.5.1 acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34064479&form=6&db=m Role of RNA in Molecular Diagnosis of MADD Patients. causal interaction,unassigned 4,0 1.5.5.1 Appendicitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28851284&form=6&db=m Anesthetic management of a pediatric patient with Electron Transfer Flavoprotein Dehydrogenase deficiency (ETFDH) and acute appendicitis: case report and review of the literature. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 beta-Thalassemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30510944&form=6&db=m Glutaric acidemia type II patient with thalassemia minor and novel electron transfer flavoprotein-A gene mutations: A case report and review of literature. causal interaction,unassigned 4,0 1.5.5.1 Carcinogenesis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29433752&form=6&db=m Irradiation of rainbow trout at early life stages results in a proteomic legacy in adult gills. Part B; the effect of a second radiation dose, after one year, on the proteomic responses in the irradiated and non-irradiated bystander fish. unassigned - 1.5.5.1 Carcinoma, Hepatocellular http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31704152&form=6&db=m Expression and significance of ETFDH in hepatocellular carcinoma. causal interaction,diagnostic usage,ongoing research,unassigned 4,3,2,0 1.5.5.1 carnitine o-palmitoyltransferase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20370797&form=6&db=m High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy. causal interaction,unassigned 3,0 1.5.5.1 carnitine o-palmitoyltransferase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28083701&form=6&db=m Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities. causal interaction,unassigned 2,0 1.5.5.1 Cerebellar Ataxia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19096106&form=6&db=m Human CoQ10 deficiencies. causal interaction,unassigned 1,0 1.5.5.1 Congenital Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29249369&form=6&db=m A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Congenital Abnormalities http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30982706&form=6&db=m Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report. causal interaction,unassigned 2,0 1.5.5.1 Deficiency Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29615056&form=6&db=m Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report. causal interaction,therapeutic application,unassigned 4,1,0 1.5.5.1 Diabetic Nephropathies http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27035869&form=6&db=m The decreased expression of electron transfer flavoprotein ? is associated with tubular cell apoptosis in diabetic nephropathy. causal interaction,unassigned 3,0 1.5.5.1 Dyslexia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12175865&form=6&db=m The Colorado mental retardation and developmental disabilities research center. causal interaction,unassigned 4,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2000260&form=6&db=m Newly identified forms of electron transfer flavoprotein deficiency in two patients with glutaric aciduria type II. causal interaction,ongoing research,therapeutic application,unassigned 3,3,1,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2082330&form=6&db=m Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2268228&form=6&db=m Defects of fatty-acid oxidation in muscle. causal interaction,unassigned 3,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2320399&form=6&db=m Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypes. causal interaction,unassigned 3,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2658591&form=6&db=m Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy. ongoing research,unassigned 2,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9889013&form=6&db=m Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism. causal interaction,diagnostic usage,unassigned 1,3,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10723193&form=6&db=m [A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)] causal interaction,diagnostic usage,therapeutic application,unassigned 3,3,1,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12175865&form=6&db=m The Colorado mental retardation and developmental disabilities research center. causal interaction,unassigned 4,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16510302&form=6&db=m Electron transfer flavoprotein deficiency: functional and molecular aspects. causal interaction,diagnostic usage,therapeutic application,unassigned 4,2,1,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17412732&form=6&db=m The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene. causal interaction,diagnostic usage,unassigned 4,4,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19592060&form=6&db=m [Multiple acyl-CoA dehydrogenase deficiency (MADD): A curable cause of genetic muscular lipidosis.] causal interaction,therapeutic application,unassigned 4,1,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20837308&form=6&db=m Glutaric aciduria type 2, late onset type in Thai siblings with myopathy. causal interaction,diagnostic usage,unassigned 4,3,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21347544&form=6&db=m Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A. causal interaction,unassigned 3,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21596162&form=6&db=m Characterization of mitochondrial proteome in a severe case of ETF-QO deficiency. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28851284&form=6&db=m Anesthetic management of a pediatric patient with Electron Transfer Flavoprotein Dehydrogenase deficiency (ETFDH) and acute appendicitis: case report and review of the literature. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 electron-transferring-flavoprotein dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33823724&form=6&db=m ETF dehydrogenase advances in molecular genetics and impact on treatment. causal interaction,unassigned 4,0 1.5.5.1 Fabry Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Genetic Diseases, Inborn http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33823724&form=6&db=m ETF dehydrogenase advances in molecular genetics and impact on treatment. causal interaction,unassigned 4,0 1.5.5.1 glycerol kinase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12175865&form=6&db=m The Colorado mental retardation and developmental disabilities research center. causal interaction,unassigned 4,0 1.5.5.1 Glycogen Storage Disease Type II http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33720849&form=6&db=m Targeted Therapies for Metabolic Myopathies Related to Glycogen Storage and Lipid Metabolism: a Systematic Review and Steps Towards a 'Treatabolome'. unassigned - 1.5.5.1 Hypoglycemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8617498&form=6&db=m Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human. causal interaction,ongoing research,therapeutic application,unassigned 4,1,1,0 1.5.5.1 Hypoglycemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17912479&form=6&db=m Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 Hypoglycemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17977044&form=6&db=m Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II. unassigned - 1.5.5.1 Hypoglycemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28914566&form=6&db=m A novel ETFDH mutation in an adult patient with late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Ichthyosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19208393&form=6&db=m Clinical and genetic analysis of lipid storage myopathies. causal interaction,unassigned 3,0 1.5.5.1 Ichthyosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20370797&form=6&db=m High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy. causal interaction,unassigned 3,0 1.5.5.1 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27113712&form=6&db=m Functional characterization of electron-transferring flavoprotein and its dehydrogenase required for fungal development and plant infection by the rice blast fungus. therapeutic application,unassigned 1,0 1.5.5.1 Leukodystrophy, Metachromatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Lipidoses http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19592060&form=6&db=m [Multiple acyl-CoA dehydrogenase deficiency (MADD): A curable cause of genetic muscular lipidosis.] causal interaction,therapeutic application,unassigned 4,1,0 1.5.5.1 medium-chain acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10723193&form=6&db=m [A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)] causal interaction,diagnostic usage,therapeutic application,unassigned 3,3,1,0 1.5.5.1 medium-chain acyl-coa dehydrogenase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20505899&form=6&db=m MR imaging findings of glutaric aciduria type II. causal interaction,unassigned 1,0 1.5.5.1 Meningitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32393189&form=6&db=m A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9334218&form=6&db=m Expression and characterization of two pathogenic mutations in human electron transfer flavoprotein. ongoing research,unassigned 1,0 1.5.5.1 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17050691&form=6&db=m Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool. causal interaction,ongoing research,unassigned 1,2,0 1.5.5.1 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20937244&form=6&db=m The electron transfer flavoprotein: Ubiquinone oxidoreductases. unassigned - 1.5.5.1 Metabolic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33732619&form=6&db=m Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screening. unassigned - 1.5.5.1 Mitochondrial Myopathies http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33304817&form=6&db=m Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients. causal interaction,diagnostic usage,unassigned 3,4,0 1.5.5.1 Movement Disorders http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2320399&form=6&db=m Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypes. causal interaction,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1430199&form=6&db=m Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patients. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1438398&form=6&db=m Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II, and identification of glycine substitution for valine 157, producing an unstable mature protein in a patient. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1438400&form=6&db=m Human cDNA encoding ETF dehydrogenase (ETF:ubiquinone oxido-reductase), and mutations in glutaric acidemia type II. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1754299&form=6&db=m Prenatal diagnosis and neonatal monitoring of a fetus with glutaric aciduria type II due to electron transfer flavoprotein (beta-subunit) deficiency. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1882842&form=6&db=m Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II--and identification of glycine substitution for valine-157 in the sequence of the precursor, producing an unstable mature protein in a patient. ongoing research,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2000260&form=6&db=m Newly identified forms of electron transfer flavoprotein deficiency in two patients with glutaric aciduria type II. causal interaction,ongoing research,therapeutic application,unassigned 3,3,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2062823&form=6&db=m Analysis of acylcarnitines in maternal urine for prenatal diagnosis of glutaric aciduria type 2. diagnostic usage,therapeutic application,unassigned 1,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2082330&form=6&db=m Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2246866&form=6&db=m A new variant of glutaric aciduria type II: deficiency of beta-subunit of electron transfer flavoprotein. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2268228&form=6&db=m Defects of fatty-acid oxidation in muscle. causal interaction,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2320399&form=6&db=m Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypes. causal interaction,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2658591&form=6&db=m Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy. ongoing research,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2989828&form=6&db=m Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3126045&form=6&db=m Recent progress in understanding glutaric acidemias. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3714057&form=6&db=m Systemic carnitine deficiency due to lack of electron transfer flavoprotein:ubiquinone oxidoreductase. ongoing research,unassigned 1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3722376&form=6&db=m The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3760196&form=6&db=m Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II. ongoing research,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6433313&form=6&db=m Glutaric aciduria type II: evidence for a defect related to the electron transfer flavoprotein or its dehydrogenase. causal interaction,diagnostic usage,unassigned 1,3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7360517&form=6&db=m Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein. causal interaction,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7586571&form=6&db=m Identification of the D-enantiomer of 2-hydroxyglutaric acid in glutaric aciduria type II. causal interaction,unassigned 1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7757062&form=6&db=m Characterization of a mutation that abolishes quinone reduction by electron transfer flavoprotein-ubiquinone oxidoreductase. ongoing research,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7912128&form=6&db=m Mutations and polymorphisms of the gene encoding the beta-subunit of the electron transfer flavoprotein in three patients with glutaric acidemia type II. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8617498&form=6&db=m Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human. causal interaction,ongoing research,therapeutic application,unassigned 4,1,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9334218&form=6&db=m Expression and characterization of two pathogenic mutations in human electron transfer flavoprotein. ongoing research,unassigned 1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10444348&form=6&db=m Assignment of electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO) to human chromosome 4q33 by fluorescence in situ hybridization and somatic cell hybridization. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10723193&form=6&db=m [A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)] causal interaction,diagnostic usage,therapeutic application,unassigned 3,3,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12359134&form=6&db=m Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12486872&form=6&db=m Molecular study of electron transfer flavoprotein alpha-subunit deficiency in two Japanese children with different phenotypes of glutaric acidemia type II. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12706375&form=6&db=m Late-onset form of beta-electron transfer flavoprotein deficiency. causal interaction,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16165386&form=6&db=m Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiency. causal interaction,ongoing research,unassigned 2,2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16510302&form=6&db=m Electron transfer flavoprotein deficiency: functional and molecular aspects. causal interaction,diagnostic usage,therapeutic application,unassigned 4,2,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17050691&form=6&db=m Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool. causal interaction,ongoing research,unassigned 1,2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17412732&form=6&db=m The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene. causal interaction,diagnostic usage,unassigned 4,4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17912479&form=6&db=m Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17977044&form=6&db=m Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19249206&form=6&db=m ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,unassigned 2,2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19265687&form=6&db=m Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19774399&form=6&db=m Characterizing the transcriptional regulation of let-721, a Caenorhabditis elegans homolog of human electron flavoprotein dehydrogenase. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20138856&form=6&db=m High resolution melting analysis facilitates mutation screening of ETFDH gene: applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20392676&form=6&db=m In vitro probe acylcarnitine profiling assay using cultured fibroblasts and electrospray ionization tandem mass spectrometry predicts severity of patients with glutaric aciduria type 2. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20505899&form=6&db=m MR imaging findings of glutaric aciduria type II. causal interaction,unassigned 1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20674745&form=6&db=m Mutational hotspots in electron transfer flavoprotein underlie defective folding and function in multiple acyl-CoA dehydrogenase deficiency. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20837308&form=6&db=m Glutaric aciduria type 2, late onset type in Thai siblings with myopathy. causal interaction,diagnostic usage,unassigned 4,3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20937244&form=6&db=m The electron transfer flavoprotein: Ubiquinone oxidoreductases. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21088898&form=6&db=m Novel ETF dehydrogenase mutations in a patient with mild glutaric aciduria type II and complex II-III deficiency in liver and muscle. causal interaction,ongoing research,unassigned 4,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21321959&form=6&db=m Subacute myopathy in a mature patient due to multiple acyl-coenzyme A dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21347544&form=6&db=m Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A. causal interaction,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21596162&form=6&db=m Characterization of mitochondrial proteome in a severe case of ETF-QO deficiency. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22190129&form=6&db=m Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23106979&form=6&db=m A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23893693&form=6&db=m Novel ETFDH mutation and imaging findings in an adult with glutaric aciduria type II. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24357026&form=6&db=m Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,unassigned 3,3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25200064&form=6&db=m Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency. causal interaction,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25913573&form=6&db=m A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency (MADD) with a novel mutation in ETFDH gene. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27000805&form=6&db=m Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,therapeutic application,unassigned 3,2,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28083701&form=6&db=m Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28851284&form=6&db=m Anesthetic management of a pediatric patient with Electron Transfer Flavoprotein Dehydrogenase deficiency (ETFDH) and acute appendicitis: case report and review of the literature. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28899466&form=6&db=m [Clinical features and ETFDH mutations of children with late-onset glutaric aciduria type II: a report of two cases]. causal interaction,diagnostic usage,therapeutic application,unassigned 2,4,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28914566&form=6&db=m A novel ETFDH mutation in an adult patient with late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28950901&form=6&db=m Compound heterozygous mutations in electron transfer flavoprotein dehydrogenase identified in a young Chinese woman with late-onset glutaric aciduria type II. causal interaction,therapeutic application,unassigned 3,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29046209&form=6&db=m [Paroxysmal muscle weakness, liver enlargement, and hypoglycemia in a boy]. causal interaction,diagnostic usage,unassigned 1,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29249369&form=6&db=m A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29615056&form=6&db=m Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report. causal interaction,therapeutic application,unassigned 4,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29988809&form=6&db=m Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30003820&form=6&db=m Coenzyme Q10 serves to couple mitochondrial oxidative phosphorylation and fatty acid ?-oxidation, and attenuates NLRP3 inflammasome activation. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30022752&form=6&db=m [A novel mutation in the ETFDH gene of an infant with multiple acyl-CoA dehydrogenase deficiency]. causal interaction,diagnostic usage,unassigned 4,4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30027710&form=6&db=m Clinical Features of Multiple Acyl-CoA Dehydrogenase Deficiency With ETFDH Variants in the First Korean Cases. diagnostic usage,unassigned 3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30424791&form=6&db=m Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30508893&form=6&db=m Long-term outcomes of a patient with late-onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutations in ETFDH: A case report. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30709034&form=6&db=m ETF-QO Mutants Uncoupled Fatty Acid ?-Oxidation and Mitochondrial Bioenergetics Leading to Lipid Pathology. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30982706&form=6&db=m Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31058673&form=6&db=m Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31392824&form=6&db=m FLAD1-associated multiple acyl-CoA dehydrogenase deficiency identified by newborn screening. causal interaction,diagnostic usage,unassigned 4,3,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31852447&form=6&db=m Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations. causal interaction,therapeutic application,unassigned 3,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31997039&form=6&db=m Multiple acyl-COA dehydrogenase deficiency in elderly carriers. ongoing research,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32064983&form=6&db=m Skin damage in a patient with lipid storage myopathy with a novel ETFDH mutation responsive to riboflavin. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32292771&form=6&db=m A Synonymous Variant c.579A>G in the ETFDH Gene Caused Exon Skipping in a Patient With Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Case Report. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32393189&form=6&db=m A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32499892&form=6&db=m Correlation between ETFDH mutations and dysregulation of serum myomiRs in MADD patients. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32925727&form=6&db=m Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: A case report and a literature review. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32959991&form=6&db=m Prenatal and foetal autopsy findings in glutaric aciduria type II. causal interaction,unassigned 2,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33131365&form=6&db=m A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33279678&form=6&db=m Disorders of flavin adenine dinucleotide metabolism: MADD and related deficiencies. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33438237&form=6&db=m CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,therapeutic application,unassigned 3,1,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33720849&form=6&db=m Targeted Therapies for Metabolic Myopathies Related to Glycogen Storage and Lipid Metabolism: a Systematic Review and Steps Towards a 'Treatabolome'. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33732619&form=6&db=m Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screening. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33778984&form=6&db=m The diagnostic potential of targeted imaging of the fetal pancreas. unassigned - 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33823724&form=6&db=m ETF dehydrogenase advances in molecular genetics and impact on treatment. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34064479&form=6&db=m Role of RNA in Molecular Diagnosis of MADD Patients. causal interaction,unassigned 4,0 1.5.5.1 Multiple Acyl Coenzyme A Dehydrogenase Deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34066864&form=6&db=m Characterization of ETFDH and PHGDH Mutations in a Patient with Mild Glutaric Aciduria Type II and Serine Deficiency. causal interaction,unassigned 4,0 1.5.5.1 Muscle Weakness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19592060&form=6&db=m [Multiple acyl-CoA dehydrogenase deficiency (MADD): A curable cause of genetic muscular lipidosis.] causal interaction,therapeutic application,unassigned 4,1,0 1.5.5.1 Muscle Weakness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25913573&form=6&db=m A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency (MADD) with a novel mutation in ETFDH gene. causal interaction,unassigned 4,0 1.5.5.1 Muscle Weakness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26821934&form=6&db=m Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 3,0 1.5.5.1 Muscle Weakness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28914566&form=6&db=m A novel ETFDH mutation in an adult patient with late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Muscle Weakness http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30681493&form=6&db=m Clinical and muscle magnetic resonance image findings in patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,therapeutic application,unassigned 4,1,1,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19096106&form=6&db=m Human CoQ10 deficiencies. causal interaction,unassigned 1,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19208393&form=6&db=m Clinical and genetic analysis of lipid storage myopathies. causal interaction,unassigned 3,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19758981&form=6&db=m Riboflavin responsive lipid storage myopathy caused by ETFDH gene mutations. causal interaction,diagnostic usage,ongoing research,therapeutic application 4,4,1,1 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20370797&form=6&db=m High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy. causal interaction,unassigned 3,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21844807&form=6&db=m Coenzyme Q deficiency in muscle. causal interaction,diagnostic usage,unassigned 1,3,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23628458&form=6&db=m Increased muscle coenzyme Q10 in riboflavin responsive MADD with ETFDH gene mutations due to secondary mitochondrial proliferation. unassigned - 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24357026&form=6&db=m Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,unassigned 3,3,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27000805&form=6&db=m Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,diagnostic usage,therapeutic application,unassigned 3,2,1,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27270537&form=6&db=m Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations. causal interaction,unassigned 1,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28456887&form=6&db=m Heterogeneous Phenotypes in Lipid Storage Myopathy Due to ETFDH Gene Mutations. causal interaction,unassigned 3,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31306230&form=6&db=m Two novel ETFDH mutations in a patient with lipid storage myopathy. causal interaction,unassigned 3,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31331668&form=6&db=m Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency. causal interaction,unassigned 3,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31852447&form=6&db=m Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations. causal interaction,therapeutic application,unassigned 3,1,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31997039&form=6&db=m Multiple acyl-COA dehydrogenase deficiency in elderly carriers. ongoing research,unassigned 2,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32064983&form=6&db=m Skin damage in a patient with lipid storage myopathy with a novel ETFDH mutation responsive to riboflavin. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33131365&form=6&db=m A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene. causal interaction,unassigned 4,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33304817&form=6&db=m Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients. causal interaction,diagnostic usage,unassigned 3,4,0 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33720849&form=6&db=m Targeted Therapies for Metabolic Myopathies Related to Glycogen Storage and Lipid Metabolism: a Systematic Review and Steps Towards a 'Treatabolome'. unassigned - 1.5.5.1 Muscular Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33823107&form=6&db=m Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China. causal interaction,diagnostic usage,unassigned 4,3,0 1.5.5.1 Muscular Dystrophies http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24920607&form=6&db=m Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies. causal interaction,diagnostic usage,unassigned 1,3,0 1.5.5.1 Muscular Dystrophies, Limb-Girdle http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33304817&form=6&db=m Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients. causal interaction,diagnostic usage,unassigned 3,4,0 1.5.5.1 Myotonia Congenita http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33304817&form=6&db=m Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients. causal interaction,diagnostic usage,unassigned 3,4,0 1.5.5.1 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20622334&form=6&db=m [Proteomic analysis of morphine rabbit myocardium with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry] diagnostic usage,unassigned 2,0 1.5.5.1 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29433752&form=6&db=m Irradiation of rainbow trout at early life stages results in a proteomic legacy in adult gills. Part B; the effect of a second radiation dose, after one year, on the proteomic responses in the irradiated and non-irradiated bystander fish. unassigned - 1.5.5.1 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31704152&form=6&db=m Expression and significance of ETFDH in hepatocellular carcinoma. causal interaction,diagnostic usage,ongoing research,unassigned 4,3,2,0 1.5.5.1 Obesity http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20859605&form=6&db=m Proteomic analysis of mitochondrial proteins in a mouse model of type 2 diabetes. causal interaction,diagnostic usage,unassigned 2,2,0 1.5.5.1 Perinatal Death http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17912479&form=6&db=m Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature. causal interaction,therapeutic application,unassigned 2,1,0 1.5.5.1 Peroxisomal Disorders http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Pick Disease of the Brain http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 pyruvate dehydrogenase (nadp+) deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Pyruvate Dehydrogenase Complex Deficiency Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Refsum Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Respiratory Insufficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31058673&form=6&db=m Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Rhabdomyolysis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31058673&form=6&db=m Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency. causal interaction,unassigned 4,0 1.5.5.1 Sepsis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32393189&form=6&db=m A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family. causal interaction,ongoing research,unassigned 4,2,0 1.5.5.1 Sphingolipidoses http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12175865&form=6&db=m The Colorado mental retardation and developmental disabilities research center. causal interaction,unassigned 4,0 1.5.5.1 Starvation http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16055629&form=6&db=m The critical role of Arabidopsis electron-transfer flavoprotein:ubiquinone oxidoreductase during dark-induced starvation. causal interaction,unassigned 1,0 1.5.5.1 Starvation http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31185291&form=6&db=m Evaluation and validation of experimental condition-specific reference genes for normalization of gene expression in Asia II-I Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae). causal interaction,therapeutic application,unassigned 1,1,0 1.5.5.1 Tangier Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0 1.5.5.1 Xanthomatosis, Cerebrotendinous http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23452774&form=6&db=m [Inborn errors of metabolism in adult neurology]. causal interaction,therapeutic application,unassigned 3,2,0