Human Disease and Mouse Model Detail
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Human Disease
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Myasthenic Syndrome, Congenital, Associated with Episodic Apnea
OMIM ID: 254210
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Synonyms
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Cms Ia2;
CMS-EA;
Congenital Myasthenic Syndrome Type Ia2; CMS1A2;
Myasthenia Gravis, Familial Infantile, 2, Formerly; FIMG2, FORMERLY;
Myasthenia, Familial Infantile; FIM;
Myasthenic Syndrome, Presynaptic, Congenital, Associated with Episodic Apnea
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Chat
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CHAT*
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1:1 Homology
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Analysis Tools