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276700
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TYROSINEMIA, TYPE I
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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, Metabolic
Renal Osteodystrophy
Rickets
Renal Osteodystrophy
Digestive System Diseases
Biliary Tract Diseases
Digestive System Neoplasms
Liver Neoplasms
Carcinoma, Hepatocellular
Gastrointestinal Diseases
Intestinal Diseases
Intestinal Obstruction
Ileus
Intestinal Pseudo-Obstruction
Liver Diseases
Hepatomegaly
Liver Cirrhosis
Liver Neoplasms
Carcinoma, Hepatocellular
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Tyrosinemias
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypertonia
Pain
Sensation Disorders
Somatosensory Disorders
Hypesthesia
Neuromuscular Diseases
Peripheral Nervous System Diseases
Eye Diseases
Eye Diseases, Hereditary
Albinism
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Osteodystrophy
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Renal Aminoacidurias
Urination Disorders
Glycosuria
Proteinuria
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Osteodystrophy
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Renal Aminoacidurias
Urination Disorders
Glycosuria
Proteinuria
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Platelet Disorders
Thrombocytopenia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Albinism
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Tyrosinemias
Brain Diseases, Metabolic, Inborn
Tyrosinemias
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type I
Porphyrias
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Renal Aminoacidurias
Skin Diseases, Genetic
Albinism
Infant, Newborn, Diseases
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Skin Diseases, Genetic
Albinism
Skin Diseases, Metabolic
Porphyrias
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Tyrosinemias
Calcium Metabolism Disorders
Rickets
Renal Osteodystrophy
Glucose Metabolism Disorders
Glycosuria
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Tyrosinemias
Brain Diseases, Metabolic, Inborn
Tyrosinemias
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type I
Porphyrias
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Renal Aminoacidurias
Porphyrias
Skin Diseases, Metabolic
Porphyrias
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin D Deficiency
Rickets
Renal Osteodystrophy
Endocrine System Diseases
Parathyroid Diseases
Hyperparathyroidism
Hyperparathyroidism, Secondary
Renal Osteodystrophy
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Hepatomegaly
Splenomegaly
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Acute Disease
Chronic Disease
Hyperplasia
Postoperative Complications
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypertonia
Pain
Sensation Disorders
Somatosensory Disorders
Hypesthesia
Pain
Signs and Symptoms, Digestive
Vomiting
Urological Manifestations
Proteinuria
Wounds and Injuries
Self Mutilation
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