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248510
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MANNOSIDOSIS, BETA A, LYSOSOMAL
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Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Tourette Syndrome
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Epilepsy
Movement Disorders
Tic Disorders
Tourette Syndrome
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Tourette Syndrome
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Sensation Disorders
Hearing Disorders
Hearing Loss
Neuromuscular Diseases
Peripheral Nervous System Diseases
Cardiovascular Diseases
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Fabry Disease
Heredodegenerative Disorders, Nervous System
Tourette Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Carbohydrate Metabolism, Inborn Errors
Mannosidase Deficiency Diseases
alpha-Mannosidosis
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Mannosidase Deficiency Diseases
alpha-Mannosidosis
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Lipid Metabolism Disorders
Lipidoses
Sphingolipidoses
Fabry Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Carbohydrate Metabolism, Inborn Errors
Mannosidase Deficiency Diseases
alpha-Mannosidosis
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Mannosidase Deficiency Diseases
alpha-Mannosidosis
Animal Diseases
Cattle Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Sensation Disorders
Hearing Disorders
Hearing Loss
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