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Results 1 - 5 of 5 for "3-methylglutaconic" aciduria type 1
  1. 3-methylglutaconyl-CoA hydratase deficiency 
    ... MGCA1 Primary 3-methylglutaconic aciduria Genetic Testing Registry: 3-Methylglutaconic aciduria type 1 3-methylglutaconic aciduria type 1 National Organization for ...
    https://medlineplus.gov/...methylglutaconyl-coa-hydratase-deficiency - Genetics
  2. Costeff syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/costeff-syndrome - Genetics
  3. Barth syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  4. Dilated cardiomyopathy with ataxia syndrome 
    ... 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 ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  5. MEGDEL syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics