Vezi şi
| Boli A-Z | | 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome
Acquired Fructose Intolerance
Acute Liver Failure
Adenocarcinoma of the Gallbladder and Extrahepatic Biliary Tract
Adenocarcinoma of the Liver and Intrahepatic Biliary Tract
Adenosquamous Bile Duct Carcinoma
Adult Endodermal Sinus Tumor
Adult Hepatocellular Carcinoma
Adult-Onset Citrullinemia Type I
Aflatoxins-Related Hepatocellular Carcinoma
Alagille Syndrome 1
Alagille Syndrome 2
Alcoholic Hepatitis
Alcoholic Liver Cirrhosis
Alpha-1-Antitrypsin Deficiency
Anemia, Hypochromic Microcytic, with Iron Overload 1
Anemia, Hypochromic Microcytic, with Iron Overload 2
Autoimmune Hepatitis
Bile Acid Coa Ligase Deficiency and Defective Amidation
Bile Acid Malabsorption, Primary
Bile Acid Synthesis Defect, Congenital, 1
Bile Acid Synthesis Defect, Congenital, 2
Bile Acid Synthesis Defect, Congenital, 3
Bile Acid Synthesis Defect, Congenital, 4
Bile Acid Synthesis Defect, Congenital, 5
Bile Acid Synthesis Defect, Congenital, 6
Bile and Pancreatic Ducts, Complete Absence of
Bile Duct Adenocarcinoma
Bile Duct Carcinoma
Bile Duct Carcinoma in Situ
Bile Duct Clear Cell Adenocarcinoma
Bile Duct Cystadenocarcinoma
Bile Duct Cystadenoma
Bile Duct Cysts
Bile Duct Disease
Bile Duct Mucinous Adenocarcinoma
Bile Duct Mucoepidermoid Carcinoma
Bile Duct Rhabdomyosarcoma
Bile Duct Sarcoma
Bile Duct Signet Ring Cell Carcinoma
Bile Reflux
Biliary Atresia
Biliary Atresia, Extrahepatic
Biliary Atresia with Splenic Malformation Syndrome
Biliary Cirrhosis, Primary, 1
Biliary Cirrhosis, Primary, 2
Biliary Cirrhosis, Primary, 3
Biliary Cirrhosis, Primary, 4
Biliary Cirrhosis, Primary, 5
Biliary Papillomatosis
Biliary Tract Neoplasm
Bladder Hepatoid Adenocarcinoma
Budd-Chiari Syndrome
Carnitine Palmitoyltransferase I Deficiency
Carnitine Palmitoyltransferase Ii Deficiency, Infantile
Caroli Disease
Caroli Disease, Isolated
Cerebellar Vermis Aplasia with Associated Features Suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome
Cerebrotendinous Xanthomatosis
Childhood Hepatocellular Carcinoma
Cholangiocarcinoma
Cholangitis, Primary Sclerosing
Cholestasis
Cholestasis, Benign Recurrent Intrahepatic, 1
Cholestasis, Benign Recurrent Intrahepatic, 2
Cholestasis-Lymphedema Syndrome
Cholestasis, Progressive Familial Intrahepatic, 1
Cholestasis, Progressive Familial Intrahepatic, 2
Cholestasis, Progressive Familial Intrahepatic, 3
Cholestasis, Progressive Familial Intrahepatic, 4
Cholestasis, Progressive Familial Intrahepatic, 5
Cirrhotic Cardiomyopathy
Citrullinemia, Type Ii, Adult-Onset
Clonorchiasis
Coach Syndrome
Combined Oxidative Phosphorylation Deficiency 1
Common Bile Duct Disease
Common Bile Duct Neoplasm
Congenital Anomaly of Hepatic Vein
Congenital Bile Acid Synthesis Defect
Congenital Bronchobiliary Fistula
Congenital Disorder of Deglycosylation
Congenital Disorder of Glycosylation, Type Ia
Congenital Disorder of Glycosylation, Type Ib
Congenital Disorder of Glycosylation, Type Ic
Congenital Disorder of Glycosylation, Type Id
Congenital Disorder of Glycosylation, Type Ie
Congenital Disorder of Glycosylation, Type if
Congenital Disorder of Glycosylation, Type Ig
Congenital Disorder of Glycosylation, Type Ih
Congenital Disorder of Glycosylation, Type Ii
Congenital Disorder of Glycosylation, Type Iia
Congenital Disorder of Glycosylation, Type Iib
Congenital Disorder of Glycosylation, Type Iic
Congenital Disorder of Glycosylation, Type Iid
Congenital Disorder of Glycosylation, Type Iif
Congenital Disorder of Glycosylation, Type Iig
Congenital Disorder of Glycosylation, Type Iih
Congenital Disorder of Glycosylation, Type Iii
Congenital Disorder of Glycosylation, Type I/iix
Congenital Disorder of Glycosylation, Type Iij
Congenital Disorder of Glycosylation, Type Iik
Congenital Disorder of Glycosylation, Type Iil
Congenital Disorder of Glycosylation, Type Iim
Congenital Disorder of Glycosylation, Type Iin
Congenital Disorder of Glycosylation, Type Iio
Congenital Disorder of Glycosylation, Type Iip
Congenital Disorder of Glycosylation, Type Iiq
Congenital Disorder of Glycosylation, Type Ij
Congenital Disorder of Glycosylation, Type Ik
Congenital Disorder of Glycosylation, Type Il
Congenital Disorder of Glycosylation, Type Im
Congenital Disorder of Glycosylation, Type in
Congenital Disorder of Glycosylation, Type Io
Congenital Disorder of Glycosylation, Type Ip
Congenital Disorder of Glycosylation, Type Iq
Congenital Disorder of Glycosylation, Type Ir
Congenital Disorder of Glycosylation, Type It
Congenital Disorder of Glycosylation, Type Iu
Congenital Disorder of Glycosylation, Type Iw
Congenital Disorder of Glycosylation, Type Ix
Congenital Disorder of Glycosylation, Type Iy
Congenital Hepatic Fibrosis
Congenital Portosystemic Shunt
Coproporphyria, Hereditary
Crigler-Najjar Syndrome, Type I
Crigler-Najjar Syndrome, Type Ii
Cystic Echinococcosis
Cystic Fibrosis
Cytochrome C Oxidase, Subunit 7a2, Pseudogene 2
Deafness, Dystonia, and Cerebral Hypomyelination
Deoxyguanosine Kinase Deficiency
Distal Biliary Tract Carcinoma
Drug-Induced Hepatitis
Dubin-Johnson Syndrome
Dykes Markes Harper Syndrome
Dystonia/parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease
Echinococcosis
Embryonal Extrahepatic Bile Duct Rhabdomyosarcoma
Endodermal Sinus Tumor
Epileptic Encephalopathy, Early Infantile, 1
Epileptic Encephalopathy, Early Infantile, 11
Epileptic Encephalopathy, Early Infantile, 12
Epileptic Encephalopathy, Early Infantile, 13
Epileptic Encephalopathy, Early Infantile, 14
Epileptic Encephalopathy, Early Infantile, 15
Epileptic Encephalopathy, Early Infantile, 16
Epileptic Encephalopathy, Early Infantile, 17
Epileptic Encephalopathy, Early Infantile, 18
Epileptic Encephalopathy, Early Infantile, 19
Epileptic Encephalopathy, Early Infantile, 2
Epileptic Encephalopathy, Early Infantile, 21
Epileptic Encephalopathy, Early Infantile, 23
Epileptic Encephalopathy, Early Infantile, 24
Epileptic Encephalopathy, Early Infantile, 25
Epileptic Encephalopathy, Early Infantile, 26
Epileptic Encephalopathy, Early Infantile, 27
Epileptic Encephalopathy, Early Infantile, 28
Epileptic Encephalopathy, Early Infantile, 29
Epileptic Encephalopathy, Early Infantile, 3
Epileptic Encephalopathy, Early Infantile, 30
Epileptic Encephalopathy, Early Infantile, 31
Epileptic Encephalopathy, Early Infantile, 32
Epileptic Encephalopathy, Early Infantile, 33
Epileptic Encephalopathy, Early Infantile, 34
Epileptic Encephalopathy, Early Infantile, 35
Epileptic Encephalopathy, Early Infantile, 36
Epileptic Encephalopathy, Early Infantile, 37
Epileptic Encephalopathy, Early Infantile, 38
Epileptic Encephalopathy, Early Infantile, 39
Epileptic Encephalopathy, Early Infantile, 4
Epileptic Encephalopathy, Early Infantile, 40
Epileptic Encephalopathy, Early Infantile, 41
Epileptic Encephalopathy, Early Infantile, 42
Epileptic Encephalopathy, Early Infantile, 43
Epileptic Encephalopathy, Early Infantile, 44
Epileptic Encephalopathy, Early Infantile, 45
Epileptic Encephalopathy, Early Infantile, 46
Epileptic Encephalopathy, Early Infantile, 47
Epileptic Encephalopathy, Early Infantile, 48
Epileptic Encephalopathy, Early Infantile, 49
Epileptic Encephalopathy, Early Infantile, 5
Epileptic Encephalopathy, Early Infantile, 50
Epileptic Encephalopathy, Early Infantile, 51
Epileptic Encephalopathy, Early Infantile, 52
Epileptic Encephalopathy, Early Infantile, 53
Epileptic Encephalopathy, Early Infantile, 54
Epileptic Encephalopathy, Early Infantile, 55
Epileptic Encephalopathy, Early Infantile, 56
Epileptic Encephalopathy, Early Infantile, 57
Epileptic Encephalopathy, Early Infantile, 58
Epileptic Encephalopathy, Early Infantile, 6
Epileptic Encephalopathy, Early Infantile, 7
Epileptic Encephalopathy, Early Infantile, 8
Epileptic Encephalopathy, Early Infantile, 9
Erythrocyte Galactose Epimerase Deficiency
Extrahepatic Bile Duct Adenocarcinoma
Extrahepatic Bile Duct Adenoma
Extrahepatic Bile Duct Cystadenoma
Extrahepatic Bile Duct Leiomyoma
Extrahepatic Bile Duct Leiomyosarcoma
Extrahepatic Bile Duct Lipoma
Extrahepatic Bile Duct Papillary Adenoma
Extrahepatic Bile Duct Small Cell Adenocarcinoma
Extrahepatic Biliary Papillomatosis
Familial Porphyria Cutanea Tarda
Fanconi-Bickel Syndrome
Fascioliasis
Fatty Liver Disease
Fatty Liver Disease, Nonalcoholic 1
Fatty Liver Disease, Nonalcoholic 2
Ferro-Cerebro-Cutaneous Syndrome
Fibrolamellar Carcinoma
Follicular Cholangitis and Pancreatitis
Fructose Intolerance, Hereditary
Fulminant Viral Hepatitis
Galactose Epimerase Deficiency
Galactosemia
Gallbladder Disease
Gallbladder Disease 1
Gallbladder Disease 2
Gallbladder Disease 3
Gallbladder Disease 4
Gallbladder Neuroendocrine Tumor
Generalized Galactose Epimerase Deficiency
Gilbert Syndrome
Glycogen Storage Disease
Glycogen Storage Disease 0, Liver
Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency
Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency
Glycogen Storage Disease Due to Liver Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ia
Glycogen Storage Disease Ib
Glycogen Storage Disease Ic
Glycogen Storage Disease Ii
Glycogen Storage Disease Iii
Glycogen Storage Disease Iv
Glycogen Storage Disease Ix
Glycogen Storage Disease Ixa
Glycogen Storage Disease Ixa1
Glycogen Storage Disease Ixb
Glycogen Storage Disease Ixc
Glycogen Storage Disease Type 0
Glycogen Storage Disease, Type Ixd
Glycogen Storage Disease V
Glycogen Storage Disease Vi
Glycogen Storage Disease Vii
Glycogen Storage Disease Viii
Glycogen Storage Disease X
Glycogen Storage Disease Xii
Glycogen Storage Disease Xiii
Glycogen Storage Disease Xv
Gracile Syndrome
Growth Retardation, Intellectual Developmental Disorder, Hypotonia, and Hepatopathy
Growth Retardation-Mild Developmental Delay-Chronic Hepatitis Syndrome
Hellp Syndrome
Hemangioma of Liver
Hemochromatosis, Neonatal
Hemochromatosis, Type 1
Hemochromatosis Type 2
Hemochromatosis, Type 2a
Hemochromatosis, Type 2b
Hemochromatosis, Type 3
Hemochromatosis, Type 4
Hemochromatosis, Type 5
Hepatic Adenomas, Familial
Hepatic Coma
Hepatic Cystic Hamartoma
Hepatic Encephalopathy
Hepatic Fibrosis, Severe Due to Schistosoma Mansoni Infection
Hepatic Infarction
Hepatic Osteogenic Sarcoma
Hepatic Tuberculosis
Hepatic Vascular Disease
Hepatic Veno-Occlusive Disease
Hepatic Venoocclusive Disease with Immunodeficiency
Hepatitis
Hepatitis a
Hepatitis B
Hepatitis B Reinfection Following Liver Transplantation
Hepatitis C
Hepatitis C Virus
Hepatitis D
Hepatitis E
Hepatoblastoma
Hepatocellular Adenoma
Hepatocellular Carcinoma
Hepatocellular Clear Cell Carcinoma
Hepatoid Adenocarcinoma
Hepatoid Pattern Ovarian Yolk Sac Tumor
Hepatoid Pattern Testicular Yolk Sac Tumor
Hepatoportal Sclerosis
Hepatopulmonary Syndrome
Hepatorenal Syndrome
Hepatosplenic T-Cell Lymphoma
Hereditary Hemorrhagic Telangiectasia
Histiocytosis-Lymphadenopathy Plus Syndrome
Hyperbilirubinemia, Rotor Type
Hyperbilirubinemia, Transient Familial Neonatal
Hyperbiliverdinemia
Hypercholanemia, Familial
Hypermanganesemia with Dystonia
Hypermanganesemia with Dystonia 1
Hypermanganesemia with Dystonia 2
Hypertriglyceridemia, Familial
Hypertriglyceridemia, Transient Infantile
Hypochromic Microcytic Anemia with Iron Overload
Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration
Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis
Idiopathic Copper-Associated Cirrhosis
Idiopathic Ductopenia
Idiopathic Malabsorption Due to Bile Acid Synthesis Defects
Idiopathic Peliosis Hepatis
Igg4-Related Hepatopathy
Igg4-Related Sclerosing Cholangitis
Il21r Immunodeficiency
Immunodeficiency 47
Infantile Epileptic Encephalopathy
Infantile Liver Failure Syndrome 1
Infantile Liver Failure Syndrome 2
Interstitial Lung and Liver Disease
Intrahepatic Bile Duct Adenoma
Intrahepatic Bile Duct Cystadenoma
Intrahepatic Biliary Papillomatosis
Intrahepatic Cholangiocarcinoma
Intrahepatic Cholestasis
Intrahepatic Gall Duct Cancer
Iron Overload in Africa
Isolated Agenesis of Gallbladder
Isolated Congenital Hepatic Fibrosis
Isolated Neonatal Sclerosing Cholangitis
Joubert Syndrome with Oculorenal Anomalies
Juvenile Hereditary Hemochromatosis
Klatskin's Tumor
Lipoatrophy with Diabetes, Leukomelanodermic Papules, Liver Steatosis, and Hypertrophic Cardiomyopathy
Liver Angiosarcoma
Liver Carcinoma in Situ
Liver Cirrhosis
Liver Disease
Liver Failure, Infantile, Transient
Liver Fibrocystic Disease and Polydactyly
Liver Fibroma
Liver Fibrosarcoma
Liver Inflammatory Pseudotumor
Liver Leiomyoma
Liver Leiomyosarcoma
Liver Lipoma
Liver Lymphoma
Liver Rhabdomyosarcoma
Liver Sarcoma
Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency
Lysosomal Acid Lipase Deficiency
Macrotrabecular Hepatoblastoma
Maturity-Onset Diabetes of the Young
Maturity-Onset Diabetes of the Young, Type 1
Maturity-Onset Diabetes of the Young, Type 10
Maturity-Onset Diabetes of the Young, Type 11
Maturity-Onset Diabetes of the Young, Type 13
Maturity-Onset Diabetes of the Young, Type 14
Maturity-Onset Diabetes of the Young, Type 2
Maturity-Onset Diabetes of the Young, Type 3
Maturity-Onset Diabetes of the Young, Type 4
Maturity-Onset Diabetes of the Young, Type 6
Maturity-Onset Diabetes of the Young, Type 7
Maturity-Onset Diabetes of the Young, Type 9
Meckel Syndrome 12
Meckel Syndrome 13
Meckel Syndrome, Type 1
Meckel Syndrome, Type 10
Meckel Syndrome, Type 11
Meckel Syndrome, Type 2
Meckel Syndrome, Type 3
Meckel Syndrome, Type 4
Meckel Syndrome, Type 5
Meckel Syndrome, Type 6
Meckel Syndrome, Type 7
Meckel Syndrome, Type 8
Meckel Syndrome, Type 9
Mitochondrial Complex Iii Deficiency, Nuclear Type 1
Mitochondrial Dna Depletion Syndrome 15
Mitochondrial Dna Depletion Syndrome 3
Mitochondrial Dna Depletion Syndrome 4a
Mitochondrial Dna Depletion Syndrome 6
Mitochondrial Dna Depletion Syndrome 7
Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form
Mixed Fibrolamellar Hepatocellular Carcinoma
Mixed Hepatoblastoma
Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome
Mulibrey Nanism
Muscular Hypertrophy-Hepatomegaly-Polyhydramnios Syndrome
Myo5b-Related Progressive Familial Intrahepatic Cholestasis
Neonatal Adrenoleukodystrophy
Nephropathy, Progressive Tubulointerstitial, with Cholestatic Liver Disease
Nodular Regenerative Hyperplasia
Nonalcoholic Steatohepatitis
North American Indian Childhood Cirrhosis
Nutmeg Liver
Opisthorchiasis
Papillary Extrahepatic Bile Duct Adenocarcinoma
Peliosis Hepatis
Perforation of Bile Duct
Perinatal Jaundice Due to Hepatocellular Damage
Peroxisome Biogenesis Disorder 10a
Peroxisome Biogenesis Disorder 10b
Peroxisome Biogenesis Disorder 11a
Peroxisome Biogenesis Disorder 11b
Peroxisome Biogenesis Disorder 12a
Peroxisome Biogenesis Disorder 13a
Peroxisome Biogenesis Disorder 14b
Peroxisome Biogenesis Disorder 1a
Peroxisome Biogenesis Disorder 1b
Peroxisome Biogenesis Disorder 2a
Peroxisome Biogenesis Disorder 2b
Peroxisome Biogenesis Disorder 3a
Peroxisome Biogenesis Disorder 3b
Peroxisome Biogenesis Disorder 4a
Peroxisome Biogenesis Disorder 4b
Peroxisome Biogenesis Disorder 5a
Peroxisome Biogenesis Disorder 5b
Peroxisome Biogenesis Disorder 6a
Peroxisome Biogenesis Disorder 6b
Peroxisome Biogenesis Disorder 7a
Peroxisome Biogenesis Disorder 7b
Peroxisome Biogenesis Disorder 8a
Peroxisome Biogenesis Disorder 8b
Peroxisome Biogenesis Disorder 9b
Polycystic Liver Disease
Polycystic Liver Disease 1
Polycystic Liver Disease 2
Polyglucosan Body Neuropathy, Adult Form
Porphyria Cutanea Tarda
Porphyria Cutanea Tarda, Type I
Portal Hypertension, Noncirrhotic
Primary Biliary Cholangitis
Primary Biliary Cirrhosis
Primary Hepatic Neuroendocrine Carcinoma
Primary Intrahepatic Lithiasis
Primitive Portal Vein Thrombosis
Pulmonary Fibrosis-Hepatic Hyperplasia-Bone Marrow Hypoplasia Syndrome
Pyruvate Kinase Deficiency, Liver Type
Recurrent Hepatitis C Virus Induced Liver Disease in Liver Transplant Recipients
Renal-Hepatic-Pancreatic Dysplasia
Renal-Hepatic-Pancreatic Dysplasia 1
Renal-Hepatic-Pancreatic Dysplasia 2
Reye Syndrome
Reynolds Syndrome
Ruijs-Aalfs Syndrome
Sclerosing Cholangitis
Sclerosing Hepatic Carcinoma
Secondary Sclerosing Cholangitis
Short Stature Cranial Hyperostosis Hepatomegaly
Short Stature, Cranial Hyperostosis, Hepatomegaly and Diabetes
Solitary Necrotic Nodule of the Liver
Spinocerebellar Ataxia 1
Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 11
Spinocerebellar Ataxia 12
Spinocerebellar Ataxia 13
Spinocerebellar Ataxia 14
Spinocerebellar Ataxia 15
Spinocerebellar Ataxia 17
Spinocerebellar Ataxia 18
Spinocerebellar Ataxia 19
Spinocerebellar Ataxia 2
Spinocerebellar Ataxia 20
Spinocerebellar Ataxia 21
Spinocerebellar Ataxia 23
Spinocerebellar Ataxia 25
Spinocerebellar Ataxia 26
Spinocerebellar Ataxia 27
Spinocerebellar Ataxia 28
Spinocerebellar Ataxia 29
Spinocerebellar Ataxia 30
Spinocerebellar Ataxia 31
Spinocerebellar Ataxia 32
Spinocerebellar Ataxia 34
Spinocerebellar Ataxia 35
Spinocerebellar Ataxia 36
Spinocerebellar Ataxia 37
Spinocerebellar Ataxia 38
Spinocerebellar Ataxia 4
Spinocerebellar Ataxia 40
Spinocerebellar Ataxia 41
Spinocerebellar Ataxia 42
Spinocerebellar Ataxia 43
Spinocerebellar Ataxia 44
Spinocerebellar Ataxia 45
Spinocerebellar Ataxia 46
Spinocerebellar Ataxia 5
Spinocerebellar Ataxia 6
Spinocerebellar Ataxia 7
Spinocerebellar Ataxia 8
Spinocerebellar Ataxia 9
Spinocerebellar Ataxia, Autosomal Recessive 1
Spinocerebellar Ataxia, Autosomal Recessive 10
Spinocerebellar Ataxia, Autosomal Recessive 11
Spinocerebellar Ataxia, Autosomal Recessive 12
Spinocerebellar Ataxia, Autosomal Recessive 13
Spinocerebellar Ataxia, Autosomal Recessive 14
Spinocerebellar Ataxia, Autosomal Recessive 15
Spinocerebellar Ataxia, Autosomal Recessive 16
Spinocerebellar Ataxia, Autosomal Recessive 17
Spinocerebellar Ataxia, Autosomal Recessive 18
Spinocerebellar Ataxia, Autosomal Recessive 2
Spinocerebellar Ataxia, Autosomal Recessive 20
Spinocerebellar Ataxia, Autosomal Recessive 21
Spinocerebellar Ataxia, Autosomal Recessive 22
Spinocerebellar Ataxia, Autosomal Recessive 23
Spinocerebellar Ataxia, Autosomal Recessive 24
Spinocerebellar Ataxia, Autosomal Recessive 25
Spinocerebellar Ataxia, Autosomal Recessive 26
Spinocerebellar Ataxia, Autosomal Recessive 3
Spinocerebellar Ataxia, Autosomal Recessive 4
Spinocerebellar Ataxia Autosomal Recessive 5
Spinocerebellar Ataxia, Autosomal Recessive 6
Spinocerebellar Ataxia, Autosomal Recessive 7
Spinocerebellar Ataxia, Autosomal Recessive 8
Spinocerebellar Ataxia Type 16
Spinocerebellar Ataxia Type 19/22
Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract
Squamous Cell Carcinoma of Liver and Intrahepatic Biliary Tract
Steroid Dehydrogenase Deficiency Dental Anomalies
Stomatin-Deficient Cryohydrocytosis with Neurologic Defects
Tang Hsi Ryu Syndrome
Telangiectasia, Hereditary Hemorrhagic, Type 1
Telangiectasia, Hereditary Hemorrhagic, Type 2
Telangiectasia, Hereditary Hemorrhagic, Type 3
Telangiectasia, Hereditary Hemorrhagic, Type 4
Telangiectasia, Hereditary Hemorrhagic, Type 5
Trichohepatoenteric Syndrome 1
Trichohepatoenteric Syndrome 2
Tyrosinemia
Tyrosinemia, Type I
Tyrosinemia, Type Ii
Tyrosinemia, Type Iii
Undifferentiated Carcinoma of Liver and Intrahepatic Biliary Tract
Undifferentiated Embryonal Sarcoma of the Liver
Viral Hepatitis
Visceral Steatosis
Visceral Steatosis, Congenital
Wilson Disease
Zimmermann-Laband Syndrome
Zimmermann-Laband Syndrome 1
Zimmermann-Laband Syndrome 2 |
|---|