Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 11 - 20 of 60 for Aciduria
  1. Dilated cardiomyopathy with ataxia syndrome 
    ... of 3-methylglutaconic acid in urine (3-methylglutaconic aciduria). People with DCMA syndrome also have high urine ... signs and symptoms of the condition. 3-methylglutaconic aciduria type V DCMA DCMA syndrome DNAJC19 defect MGA ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  2. Barth syndrome 
    ... of 3-methylglutaconic acid in urine (3-methylglutaconic aciduria).Even though most features of Barth syndrome are ... X-linked traits to their sons. 3 methylglutaconic aciduria, type II 3-methylglutaconic aciduria type 2 BTHS ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  3. MMAA gene 
    ... acidemia. More About This Health Condition cblA methylmalonic aciduria (cobalamin deficiency) cblA type methylmalonic aciduria (cobalamin deficiency) type A methylmalonic aciduria type A ...
    https://medlineplus.gov/genetics/gene/mmaa - Genetics
  4. Glutaric acidemia type I 
    Glutaric acidemia type I (also called glutaric aciduria type I) is an inherited disorder in which the body is unable to process certain proteins properly. It is classified as an organic ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  5. MMAB gene 
    ... ATR cblB CFAP23 cob(I)alamin adenosyltransferase methylmalonic aciduria (cobalamin deficiency) cblB type methylmalonic aciduria (cobalamin deficiency) type B MMAB_HUMAN Tests of ...
    https://medlineplus.gov/genetics/gene/mmab - Genetics
  6. MMACHC gene 
    ... More About This Health Condition cblC DKFZP564I122 methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria methylmalonic aciduria ...
    https://medlineplus.gov/genetics/gene/mmachc - Genetics
  7. Primary hyperoxaluria 
    ... condition. Congenital oxaluria D-glycerate dehydrogenase deficiency Glyceric aciduria Glycolic aciduria Hepatic AGT deficiency Hyperoxaluria, primary Oxalosis ...
    https://medlineplus.gov/genetics/condition/primary-hyperoxaluria - Genetics
  8. ETFA gene 
    ... alpha polypeptide electron-transfer-flavoprotein, alpha polypeptide (glutaric aciduria II) electron-transferring-flavoprotein, alpha polypeptide (glutaric aciduria ...
    https://medlineplus.gov/genetics/gene/etfa - Genetics
  9. Methylmalonic acidemia with homocystinuria 
    ... acidemia and homocystinemia Methylmalonic acidemia and homocystinuria Methylmalonic aciduria and homocystinuria Vitamin B12 metabolic defect with combined ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  10. Mevalonate kinase deficiency 
    ... HIDS) and a more severe type called mevalonic aciduria (MVA).During episodes of fever, people with HIDS ... Hyperimmunoglobulin D with periodic fever Hyperimmunoglobulinemia D Mevalonic aciduria Mevalonicaciduria Periodic fever, Dutch type Genetic Testing Registry: ...
    https://medlineplus.gov/.../condition/mevalonate-kinase-deficiency - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · next