Gendoo - MeSH tree view

MeSH Treeview

Query OMIM entry list

272750	-	TAY-SACHS DISEASE, AB VARIANT

→ High-scoring List

Musculoskeletal Diseases

Bone Diseases, Developmental

Marfan Syndrome

Nervous System Diseases

Demyelinating Diseases

Hereditary Central Nervous System Demyelinating Diseases

Leukodystrophy, Metachromatic

Neurodegenerative Diseases

Motor Neuron Disease

Muscular Atrophy, Spinal

Neurologic Manifestations

Neuromuscular Diseases

Motor Neuron Disease

Muscular Atrophy, Spinal

Muscular Atrophy, Spinal

Male Urogenital Diseases

Urologic Diseases

Urination Disorders

Female Urogenital Diseases and Pregnancy Complications

Female Urogenital Diseases

Urologic Diseases

Urination Disorders

Cardiovascular Diseases

Cardiovascular Abnormalities

Heart Defects, Congenital

Marfan Syndrome

Heart Defects, Congenital

Marfan Syndrome

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Congenital Abnormalities

Abnormalities, Multiple

Marfan Syndrome

Cardiovascular Abnormalities

Heart Defects, Congenital

Marfan Syndrome

Skin and Connective Tissue Diseases

Connective Tissue Diseases

Marfan Syndrome

Nutritional and Metabolic Diseases

Metabolic Diseases

Brain Diseases, Metabolic

Brain Diseases, Metabolic, Inborn

Hereditary Central Nervous System Demyelinating Diseases

Leukodystrophy, Metachromatic

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Tay-Sachs Disease

Sandhoff Disease

Leukodystrophy, Metachromatic

Lipid Metabolism Disorders

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Tay-Sachs Disease

Leukodystrophy, Metachromatic

Nutrition Disorders

Deficiency Diseases

Protein Deficiency

Animal Diseases

Disease Models, Animal

Pathological Conditions, Signs and Symptoms

Signs and Symptoms

Neurologic Manifestations

Urological Manifestations

Database Center for Life Science