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Results 11 - 20 of 33 for Metabolic syndrome X
  1. Trimethylaminuria 
    ... J. Trimethylaminuria: an under-recognised and socially debilitating metabolic disorder. J ... the fish malodor syndrome. Drug Metab Dispos. 2001 Apr;29(4 Pt ...
    https://medlineplus.gov/genetics/condition/trimethylaminuria - Genetics
  2. CHILD syndrome 
    ... PubMed Herman GE. Disorders of cholesterol biosynthesis: prototypic metabolic ... No abstract available. Citation on PubMed Kim CA, ...
    https://medlineplus.gov/genetics/condition/child-syndrome - Genetics
  3. Small fiber neuropathy 
    ... neuropathy. Other causes of this condition include a metabolic disorder called Fabry disease, immune disorders such as celiac ... Faber CG, Hoeijmakers JG, Ahn HS, Cheng X, Han C, Choi JS, Estacion M, Lauria G, ...
    https://medlineplus.gov/genetics/condition/small-fiber-neuropathy - Genetics
  4. Kearns-Sayre syndrome 
    ... doi: 10.1046/j.1432-1327.1998.2570192.x. Citation on PubMed ... Apr 15. Citation on PubMed
    https://medlineplus.gov/genetics/condition/kearns-sayre-syndrome - Genetics
  5. Mitochondrial DNA 
    ... Klockgether T, Kunz WS. New insights into the metabolic consequences of ... migraine headache and cyclic vomiting syndrome. Am J Med Genet A. 2004 Nov 15; ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  6. Lowe syndrome 
    ... to increased urination, dehydration, and abnormally acidic blood (metabolic acidosis). A ... This condition is inherited in an X-linked pattern. A condition is considered X-linked ...
    https://medlineplus.gov/genetics/condition/lowe-syndrome - Genetics
  7. Barth syndrome 
    ... Barth syndrome is one of a group of metabolic disorders that can be diagnosed by the presence ... is inherited in an X-linked recessive pattern. The gene associated with this ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  8. Gitelman syndrome 
    Gitelman syndrome is a kidney disorder that causes an imbalance of charged atoms (ions) in the body, including ions of potassium, magnesium, and calcium.The signs ...
    https://medlineplus.gov/genetics/condition/gitelman-syndrome - Genetics
  9. Cutis laxa 
    ... laxa, autosomal recessive Genetic Testing Registry: Cutis laxa, X-linked ... Citation on PubMed Kaler SG. Metabolic and molecular bases of Menkes disease and occipital ...
    https://medlineplus.gov/genetics/condition/cutis-laxa - Genetics
  10. LIMK1 gene 
    ... 69. doi: 10.1016/s0092-8674(00)80077-x. Citation on PubMed ... and metabolic abnormalities of the hippocampal formation in Williams syndrome. ...
    https://medlineplus.gov/genetics/gene/limk1 - Genetics
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