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Results 91 - 100 of 120 for Blood group B
  1. Glutaric acidemia type II 
    ... MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY; MADD PubMed Angle B, Burton BK. Risk of sudden death and acute ... V, Vilaseca MA, Campistol J, Osorio JH, Andresen BS, Gregersen N. Late-onset form of beta-electron ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-ii - Genetics
  2. Cryptogenic cirrhosis 
    ... of appetite, weight loss, nausea, swelling (edema), enlarged blood vessels, and yellowing of the skin and whites ... jaundice).People with cryptogenic cirrhosis may develop high blood pressure in the vein that supplies blood to ...
    https://medlineplus.gov/genetics/condition/cryptogenic-cirrhosis - Genetics
  3. Rheumatoid arthritis 
    ... symptoms in people who have the disease. HLA-B HLA-DPB1 HLA-DRB1 IRF5 PTPN22 RBPJ RUNX1 ... ARTHRITIS; RA PubMed Carmona L, Cross M, Williams B, Lassere M, March L. Rheumatoid arthritis. Best Pract ...
    https://medlineplus.gov/genetics/condition/rheumatoid-arthritis - Genetics
  4. Gaucher disease 
    ... and spleen (hepatosplenomegaly), a low number of red blood cells (anemia), easy bruising caused by a decrease in blood platelets (thrombocytopenia), bone abnormalities such as bone pain ...
    https://medlineplus.gov/genetics/condition/gaucher-disease -
  5. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... and symptoms include lack of energy (lethargy), low blood glucose (hypoglycemia), weak muscle tone (hypotonia), delayed development ... CK, Treem WR, Hale DE, Bennett MJ, Gibson B, Shapiro S, Strauss AW. The molecular basis of ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  6. Heterotaxy syndrome 
    ... on PubMed El Malti R, Liu H, Doray B, Thauvin C, Maltret A, Dauphin C, Goncalves-Rocha ... SD, Gaynor JW, Krogmann ON, Kurosawa H, Maruszewski B, Stellin G, Elliott MJ. The nomenclature, definition and ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  7. 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... also have muscle weakness (hypotonia), liver problems, low blood glucose (hypoglycemia), and abnormally high levels of insulin ( ... the amount of glucose that moves from the blood into cells for conversion to energy. Individuals with ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  8. Medium-chain acyl-CoA dehydrogenase deficiency 
    ... P, Black C, Rocca A, Haas M, Wilcken B. Neuropsychological functioning in children with medium chain acyl ... Visser G, Mulder MF, Rubio-Gozalbo ME, Elvers B, Niezen-Koning KE, Wanders RJ, Waterham HR, Reijngoud ...
    https://medlineplus.gov/...m-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  9. SRD5A3-congenital disorder of glycosylation 
    ... CDG can include skin rash, unusually small red blood cells (microcytic anemia), and liver problems. SRD5A3-CDG ... 18. No abstract available. Citation on PubMed Kara B, Ayhan O, Gokcay G, Basbogaoglu N, Tolun A. ...
    https://medlineplus.gov/...d5a3-congenital-disorder-of-glycosylation - Genetics
  10. Guanidinoacetate methyltransferase deficiency 
    ... Young SP. Elevation of guanidinoacetate in newborn dried blood spots and impact of early treatment in GAMT ... S, van Karnebeek CD. Cerebral creatine deficiencies: a group of treatable intellectual developmental disorders. Semin Neurol. 2014 ...
    https://medlineplus.gov/...idinoacetate-methyltransferase-deficiency - Genetics
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