MeSH Treeview
Query OMIM entry list
230500
-
GM1-GANGLIOSIDOSIS, TYPE I
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Joint Diseases
Hip Dislocation, Congenital
Musculoskeletal Abnormalities
Hip Dislocation, Congenital
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Malabsorption Syndromes
Lactose Intolerance
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Diseases
Eye Diseases
Corneal Diseases
Corneal Opacity
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Pregnancy Complications
Fetal Diseases
Fetal Growth Retardation
Oligohydramnios
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Cardiomyopathies
Heart Failure
Heart Valve Diseases
Mitral Valve Insufficiency
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Hemic and Lymphatic Diseases
Lymphatic Diseases
Histiocytosis
Histiocytosis, Non-Langerhans-Cell
Niemann-Pick Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Musculoskeletal Abnormalities
Hip Dislocation, Congenital
Fetal Diseases
Fetal Growth Retardation
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Fabry Disease
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Alkaptonuria
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Carbohydrate Metabolism, Inborn Errors
Lactose Intolerance
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis IV
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis IV
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis IV
Skin Diseases
Pigmentation Disorders
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Malabsorption Syndromes
Lactose Intolerance
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Alkaptonuria
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Carbohydrate Metabolism, Inborn Errors
Lactose Intolerance
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis IV
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Gangliosidosis, GM1
Niemann-Pick Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis IV
Animal Diseases
Disease Models, Animal
Sheep Diseases
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Cardiomegaly
Pathologic Processes
Chromosome Aberrations
Disease Attributes
Chronic Disease
Growth Disorders
Fetal Growth Retardation
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Database Center for Life Science
