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Boli A-Z Acute Liver Failure Adenocarcinoma Agammaglobulinemia Aging Alagille Syndrome 1 Al Amyloidosis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Al-Raqad Syndrome Amyloidosis Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Atp8b1 Deficiency Autoimmune Hepatitis Bile Acid Synthesis Defect, Congenital, 1 Bile Duct Disease Biliary Atresia Biliary Atresia, Extrahepatic Biliary Tract Disease Bilirubin Metabolic Disorder Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Breast Cancer Cardiogenic Shock Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Cholangiocarcinoma Cholangitis Cholangitis, Primary Sclerosing Choledocholithiasis Cholelithiasis Cholestasis Cholestasis, Benign Recurrent Intrahepatic, 1 Cholestasis, Benign Recurrent Intrahepatic, 2 Cholestasis, Intrahepatic, of Pregnancy, 1 Cholestasis, Progressive Familial Intrahepatic, 1 Cholestasis, Progressive Familial Intrahepatic, 2 Cholestasis, Progressive Familial Intrahepatic, 3 Citrullinemia, Type Ii, Neonatal-Onset Cohen-Gibson Syndrome Colon Adenocarcinoma Cytomegalic Inclusion Disease Diabetes Insipidus Diabetes Mellitus Diarrhea Dilated Cardiomyopathy Dubin-Johnson Syndrome Eclampsia Endotheliitis Extrahepatic Cholestasis Fanconi Anemia, Complementation Group E Gestational Diabetes Hellp Syndrome Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hepatoblastoma Hepatocellular Carcinoma Hereditary Spherocytosis Hyperbilirubinemia, Rotor Type Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoglycemia Hypoxia Impetigo Impetigo Herpetiformis Liver Cirrhosis Liver Disease Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Myeloma, Multiple Myopathy Myopathy, Centronuclear, X-Linked Neonatal Jaundice Neurodegeneration with Brain Iron Accumulation 2a Neuromuscular Disease Obstructive Jaundice Ovarian Hyperstimulation Syndrome Pancreatitis Pancytopenia Paraneoplastic Syndromes Pemphigoid Gestationis Pheochromocytoma Pneumonia Polymorphic Reticulosis Portal Hypertension Pre-Eclampsia Prieto X-Linked Mental Retardation Syndrome Primary Biliary Cirrhosis Pulmonic Stenosis Pure Red-Cell Aplasia Retinitis Retinitis Pigmentosa Riddle Syndrome Sarcoidosis 2 Sclerosing Cholangitis Sialadenitis Sickle Cell Anemia Sickle Cell Disease Siderosis Spinal and Bulbar Muscular Atrophy, X-Linked 1 Steatorrhea Systemic Mastocytosis Undifferentiated Pleomorphic Sarcoma Vaginal Cancer Ventricular Fibrillation, Paroxysmal Familial, 1 Viral Hepatitis Wilson Disease X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome