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"3-Methylglutaconic" aciduria type 3
- ... not show signs and symptoms of the condition. 3-methylglutaconic aciduria type 3 3-methylglutaconic aciduria type III Autosomal recessive OPA3 Autosomal recessive optic atrophy ...
- ... not show signs and symptoms of the condition. 3-methylglutaconic aciduria type 7 3-methylglutaconic aciduria type VII 3-methylglutaconic aciduria with cataracts, neurologic involvement ...
- ... cannot pass X-linked traits to their sons. 3 methylglutaconic aciduria, type II 3-methylglutaconic aciduria type 2 BTHS Cardioskeletal myopathy with neutropenia and abnormal ...
- ... not show signs and symptoms of the condition. 3-methylglutaconic aciduria, type I 3-MG-CoA-hydratase deficiency AUH defect ... MGCA1 Primary 3-methylglutaconic aciduria Genetic Testing Registry: 3-Methylglutaconic aciduria type 1 3-methylglutaconic aciduria type 1 National Organization ...
- ... not show signs and symptoms of the condition. 3-methylglutaconic aciduria type V DCMA DCMA syndrome DNAJC19 defect MGA type V MGA5 MGCA5 Genetic Testing Registry: 3-methylglutaconic aciduria type 5 Dilated cardiomyopathy with ataxia National Organization for ...
- ... not show signs and symptoms of the condition. 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy, and Leigh-like ... hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like ...