MeSH Treeview
Query OMIM entry list
601462
SCCMS
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Muscle Weakness
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Myasthenia Gravis
Myasthenia Gravis, Neonatal
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Strabismus
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
Muscular Atrophy
Paralysis
Ophthalmoplegia
Neuromuscular Diseases
Muscular Diseases
Neuromuscular Junction Diseases
Myasthenia Gravis
Myasthenia Gravis, Neonatal
Myasthenic Syndromes, Congenital
Eye Diseases
Eyelid Diseases
Blepharoptosis
Ocular Motility Disorders
Ophthalmoplegia
Strabismus
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Myasthenic Syndromes, Congenital
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Myasthenia Gravis
Myasthenia Gravis, Neonatal
Hypersensitivity
Drug Hypersensitivity
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
Muscular Atrophy
Paralysis
Ophthalmoplegia
Database Center for Life Science
