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Results 1 - 10 of 47 for Heavy chain disease
  1. Heavy Chain Diseases (Merck & Co., Inc.)  
    Blood Disorders/Specifics ... Blood Disorders ... Merck & Co., Inc. ... Heavy Chain Diseases - Learn about the causes, symptoms, diagnosis & treatment from the Merck Manuals - ...
    https://www.merckmanuals.com/.../heavy-chain-diseases - External Health Links
  2. Blood Disorders (National Library of Medicine)  
    Your blood is living tissue made up of liquid and solids. The liquid part, called plasma, is made of water, salts and protein. Over half of your blood is ...
    https://medlineplus.gov/blooddisorders.html - Health Topics
  3. Plasma Cell Disorders (Merck & Co., Inc.)  
    Blood Disorders/Specifics ... Blood Disorders ... Merck & Co., Inc. ... Overview of Plasma Cell Disorders - Explore from the Merck Manuals - Medical Consumer Version. ... light ...
    https://www.merckmanuals.com/.../overview-of-plasma-cell-disorders - External Health Links
  4. DYNC1H1 gene 
    ... protein produced from the DYNC1H1 gene is a heavy chain. Other subunits are produced from different genes. MedlinePlus Genetics provides information about Charcot-Marie-Tooth disease More About This Health Condition At least eight ...
    https://medlineplus.gov/genetics/gene/dync1h1 - Genetics
  5. Understanding Your Test Results (International Myeloma Foundation) - PDF  
    Multiple Myeloma/Diagnosis and Tests ... Multiple Myeloma ... International Myeloma Foundation ... PDF
    https://imf-d8-prod.s3.us-west-1.wasabisys.com/...-testresults_0.pdf - External Health Links
  6. AAAS gene 
    ... K, Huebner A, Clark AJ. Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanism. Mol Endocrinol. 2009 Dec;23(12):2086- ...
    https://medlineplus.gov/genetics/gene/aaas - Genetics
  7. Triple A syndrome 
    ... K, Huebner A, Clark AJ. Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanism. Mol Endocrinol. 2009 Dec;23(12):2086- ...
    https://medlineplus.gov/genetics/condition/triple-a-syndrome - Genetics
  8. CTSD gene 
    ... of two parts, one light chain and one heavy chain. At least seven mutations in the CTSD gene have been found to cause CLN10 disease. The signs and symptoms of CLN10 disease are ...
    https://medlineplus.gov/genetics/gene/ctsd - Genetics
  9. CYBB gene 
    ... kDa polypeptide p91-PHOX superoxide-generating NADPH oxidase heavy chain subunit ... S, Gougerot-Pocidalo MA, Elbim C, Grandchamp B. Molecular epidemiology of chronic granulomatous disease in a series of 80 kindreds: identification of ...
    https://medlineplus.gov/genetics/gene/cybb - Genetics
  10. MYH6 gene 
    ... Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects. PLoS One. 2011;6(12):e28872. doi: 10.1371/journal.pone.0028872. Epub 2011 Dec 14. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
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