MeSH Treeview
Query OMIM entry list
300644
GLA
GALACTOSIDASE, ALPHA
→
High-scoring List
Neoplasms
Neoplastic Processes
Neoplasm Metastasis
Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Tinnitus
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Tinnitus
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Peripheral Nervous System Diseases
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Hypertension, Renal
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Urination Disorders
Proteinuria
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Hypertension, Renal
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Urination Disorders
Proteinuria
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Hypertrophy, Left Ventricular
Cardiomyopathies
Vascular Diseases
Angiomatosis
Klippel-Trenaunay-Weber Syndrome
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Hypertension
Hypertension, Renal
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Fabry Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Muscular Dystrophies
Skin and Connective Tissue Diseases
Skin Diseases
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
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Cardiomegaly
Hypertrophy, Left Ventricular
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Disease Progression
Rare Diseases
Neoplastic Processes
Neoplasm Metastasis
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Tinnitus
Urological Manifestations
Proteinuria
Database Center for Life Science
