Phenotypes for disease #04583 (CMS9 (myasthenic syndrome, congenital, type 9, associated with acetylcholine receptor deficiency (CMS-9)), OMIM:616325)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000105422 - - - Familial, autosomal recessive - - - - - Ana Topf 00132656
0000105423 - - - Familial, autosomal recessive - - - - - Ana Topf 00132658
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