Phenotypes for disease #05223 (CMS20 (myasthenic syndrome, congenital, type 20, presynaptic (CMS-20)), OMIM:617143)

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000078531 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100311
0000078532 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100312
0000078533 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100313
0000078534 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100314
0000078535 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100315
0000078536 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100316
0000357012 Laryngeal dystonia, Laryngospasm, Involuntary movements, Central hypotonia Congenital myastenic syndrome CMS20 Isolated (sporadic) - - - - - Camille Verebi 00472203
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