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Results 1 - 9 of 9 for Potassium deficiency
  1. Beta-ketothiolase deficiency 
    ... A thiolase deficiency Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated Mitochondrial acetoacetyl-CoA thiolase deficiency T2 deficiency ...
    https://medlineplus.gov/.../condition/beta-ketothiolase-deficiency - Genetics
  2. Corticosterone methyloxidase deficiency 
    ... low levels of sodium and high levels of potassium in the blood (hyponatremia and hyperkalemia, respectively). Individuals with corticosterone methyloxidase deficiency can also have high levels of acid in ...
    https://medlineplus.gov/.../corticosterone-methyloxidase-deficiency - Genetics
  3. 17 alpha-hydroxylase/17,20-lyase deficiency 
    ... and symptoms of 17α-hydroxylase/17,20-lyase deficiency, which include high blood pressure (hypertension), low levels of potassium in the blood (hypokalemia), and abnormal sexual development. ...
    https://medlineplus.gov/...-alpha-hydroxylase-17-20-lyase-deficiency - Genetics
  4. KCNH2 gene 
    ... family of genes that provide instructions for making potassium channels. These channels, which transport positively charged atoms (ions) of potassium out of cells, play key roles in a ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  5. CYP11B2 gene 
    ... corticosterone methyloxidase deficiency (also known as aldosterone synthase ... blood and release potassium in the urine. As a result, excessive amounts ...
    https://medlineplus.gov/genetics/gene/cyp11b2 - Genetics
  6. CYP17A1 gene 
    ... known as complete 17α-hydroxylase/17,20-lyase deficiency.Without 17α-hydroxylase ... and low levels of potassium in the blood (hypokalemia).A loss of 17, ...
    https://medlineplus.gov/genetics/gene/cyp17a1 - Genetics
  7. CLPB gene 
    ... leads to the signs and symptoms of CLPB deficiency. More About This Health Condition ... ...
    https://medlineplus.gov/genetics/gene/clpb - Genetics
  8. Episodic ataxia 
    ... The protein produced from the KCNA1 gene transports potassium ions, and the protein produced from the CACNA1A ... Hanna MG. Episodic ataxia type 1: a neuronal potassium channelopathy. Neurotherapeutics. 2007 Apr;4(2):258-66. ...
    https://medlineplus.gov/genetics/condition/episodic-ataxia - Genetics
  9. SLC4A1 gene 
    ... allows positively charged molecules of sodium (Na+) and potassium (K+) to leak out of the cell. As ... gene defects in hereditary spherocytosis with band 3 deficiency. Blood. 1996 Dec 1;88(11):4366-74. ...
    https://medlineplus.gov/genetics/gene/slc4a1 - Genetics