Fatty liver disease
Metabolic abetalipoproteinemia, glycogen storage diseases, Weber-Christian disease, acute fatty liver of pregnancy, ...
ABL
... may refer to: ABL (gene), a proto-oncogene associated with chronic myelogenous leukemia Abetalipoproteinemia, a rare ...
List of MeSH codes (C10)
... abetalipoproteinemia MeSH C10.228.140.163.100.162 - carbamoyl-phosphate synthase i deficiency disease MeSH C10.228.140.163. ...
Microsome
MTP has a large use for abetalipoproteinemia patients with MTP mutations because of how it affects the assembly and secretion ...
List of MeSH codes (C18)
... abetalipoproteinemia MeSH C18.452.100.100.162 - carbamoyl-phosphate synthase I deficiency disease MeSH C18.452.100.100.175 - ... abetalipoproteinemia MeSH C18.452.648.151.162 - carbamoyl-phosphate synthase i deficiency disease MeSH C18.452.648.151.168 - ... abetalipoproteinemia MeSH C18.452.339.875.440 - hypobetalipoproteinemia MeSH C18.452.339.875.448 - lecithin acyltransferase ... abetalipoproteinemia MeSH C18.452.648.556.500.440 - hypobetalipoproteinemia MeSH C18.452.648.556.500.448 - lecithin ...
List of MeSH codes (C16)
... abetalipoproteinemia MeSH C16.320.565.150.162 - carbamoyl-phosphate synthase I deficiency disease MeSH C16.320.565.150.168 - ... abetalipoproteinemia MeSH C16.320.565.556.500.440 - hypobetalipoproteinemia MeSH C16.320.565.556.500.448 - lecithin ...
Sydenham's chorea
... abetalipoproteinemia, ataxia-telangiectasia, biotin-thiamine-responsive basal ganglia disease (BTBGD), Fahr disease, familial ...
Anemia
Abetalipoproteinemia, causing defects in membrane lipids Enzyme deficiencies Pyruvate kinase and hexokinase deficiencies, ...
List of MeSH codes (C15)
... abetalipoproteinemia MeSH C15.378.147.142 - agammaglobulinemia MeSH C15.378.147.150 - antithrombin iii deficiency MeSH C15.378. ...
List of ICD-9 codes 240-279: endocrine, nutritional and metabolic diseases, and immunity disorders
... unspecified hyperlipidemia Alpha-lipoproteinemia Combined hyperlipidemia 272.5 Lipoprotein deficiencies Abetalipoproteinemia ...
Hypocholesterolemia
... such as in celiac disease malnutrition abetalipoproteinemia - a rare genetic disease that causes cholesterol readings below 50 ...
Autosomal recessive cerebellar ataxia
... to CWF19L1 deficiency Congenital cerebellar ataxia due to RNU12 mutation Ataxia with vitamin E deficiency Abetalipoproteinemia ...