Genetics Home Reference: Abetalipoproteinemia
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Scan day: 20 February 2014 UTC
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Description: Provides information on this disorder that affects the absorption of fats, cholesterol, and fat-soluble vitamins. Includes links to other resources.
Abetalipoproteinemia - Genetics Home Reference U.S. National Library of Medicine® Quick links to this topic Information about genetic conditions and rare diseases
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| Page title: | Abetalipoproteinemia - Genetics Home Reference |
| Keywords: | abetalipoproteinemia,Hypobetalipoproteinemias,Hypolipoproteinemias,Lipid Metabolism, Inborn Errors,Metabolism, Inborn Errors,Genetic Diseases, Inborn,Congenital, Hereditary, and Neonatal Diseases and Abnormalities,Dyslipidemias,Lipid Metabolism Disorders,Metabolic Diseases,Nutritional and Metabolic Diseases,Abetalipoproteinemia,Blood/lymphatic system,Brain and nervous system,Digestive system,Eyes and vision,Food, nutrition, and metabolism,hypolipoproteinemia,MTTP,MTTP gene,Abetalipoproteinemia neuropathy,acanthocytosis,Apolipoprotein B deficiency,Bassen-Kornzweig Syndrome,Betalipoprotein Deficiency Disease,Congenital betalipoprotein deficiency syndrome,Microsomal Triglyceride Transfer Protein Deficiency Disease,National Library of Medicine,NLM,National Institutes of Health,NIH,health problem,health problems,disease,diseases,human genetics,gene,genes,genetic disease,genetic conditions,genetic disorders,medical genetics,genetics education,genetics glossary,gene reference,genetics reference |
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| IP-address: | 130.14.81.53 |
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| WHOIS | Status: ACTIVE |
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