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Query OMIM entry list
211600
PFIC1
CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Carcinoma
Adenocarcinoma
Carcinoma, Hepatocellular
Neoplasms by Site
Digestive System Neoplasms
Liver Neoplasms
Carcinoma, Hepatocellular
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Bone Diseases, Metabolic
Rickets
Digestive System Diseases
Biliary Tract Diseases
Bile Duct Diseases
Cholestasis
Cholestasis, Intrahepatic
Liver Cirrhosis, Biliary
Digestive System Neoplasms
Liver Neoplasms
Carcinoma, Hepatocellular
Gastrointestinal Diseases
Intestinal Diseases
Malabsorption Syndromes
Celiac Disease
Liver Diseases
Cholestasis, Intrahepatic
Liver Cirrhosis, Biliary
Hepatitis
Hepatolenticular Degeneration
Hepatomegaly
Liver Cirrhosis
Liver Cirrhosis, Biliary
Liver Neoplasms
Carcinoma, Hepatocellular
Respiratory Tract Diseases
Lung Diseases
Pneumonia
Respiratory Tract Infections
Pneumonia
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Hepatolenticular Degeneration
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Movement Disorders
Hepatolenticular Degeneration
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hepatolenticular Degeneration
Neurologic Manifestations
Dyskinesias
Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Eye Diseases
Corneal Diseases
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Hypoprothrombinemias
Coagulation Protein Disorders
Hypoprothrombinemias
Hemorrhagic Disorders
Hypoprothrombinemias
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hypoprothrombinemias
Dwarfism
Heredodegenerative Disorders, Nervous System
Hepatolenticular Degeneration
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Carbohydrate Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary
Jaundice, Chronic Idiopathic
Metal Metabolism, Inborn Errors
Hepatolenticular Degeneration
Infant, Newborn, Diseases
Hyperbilirubinemia, Neonatal
Jaundice, Neonatal
Jaundice, Chronic Idiopathic
Skin and Connective Tissue Diseases
Skin Diseases
Pruritus
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Calcium Metabolism Disorders
Hypocalcemia
Rickets
Glucose Metabolism Disorders
Hypoglycemia
Malabsorption Syndromes
Celiac Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Carbohydrate Metabolism, Inborn Errors
Hyperbilirubinemia, Hereditary
Jaundice, Chronic Idiopathic
Metal Metabolism, Inborn Errors
Hepatolenticular Degeneration
Water-Electrolyte Imbalance
Hypocalcemia
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin D Deficiency
Rickets
Vitamin E Deficiency
Endocrine System Diseases
Dwarfism
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Hepatomegaly
Splenomegaly
Pathologic Processes
Disease
Syndrome
Disease Attributes
Chronic Disease
Disease Progression
Recurrence
Growth Disorders
Hemorrhage
Hyperbilirubinemia
Jaundice
Signs and Symptoms
Body Weight
Neurologic Manifestations
Dyskinesias
Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Skin Manifestations
Jaundice
Pruritus
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