MeSH Treeview
Query OMIM entry list
608931
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MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
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Musculoskeletal Diseases
Joint Diseases
Arthrogryposis
Muscular Diseases
Arthrogryposis
Musculoskeletal Abnormalities
Arthrogryposis
Respiratory Tract Diseases
Respiration Disorders
Apnea
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Myasthenia Gravis
Myasthenia Gravis, Neonatal
Neuromuscular Diseases
Neuromuscular Junction Diseases
Myasthenia Gravis
Myasthenia Gravis, Neonatal
Myasthenic Syndromes, Congenital
Eye Diseases
Eyelid Diseases
Blepharoptosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Musculoskeletal Abnormalities
Arthrogryposis
Genetic Diseases, Inborn
Myasthenic Syndromes, Congenital
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Myasthenia Gravis
Myasthenia Gravis, Neonatal
Animal Diseases
Disease Models, Animal
Dog Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Facies
Signs and Symptoms
Signs and Symptoms, Respiratory
Apnea
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