MeSH Treeview
Query OMIM entry list
181430
SPMM
SCAPULOPERONEAL MYOPATHY, MYH7-RELATED
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Osteitis Deformans
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Nervous System Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Myotonic Dystrophy
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Paresis
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Myotonic Dystrophy
Muscular Dystrophies
Myotonic Dystrophy
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Paresis
Database Center for Life Science