Phenotypes for disease #04314 (CMS2C (myasthenic syndrome, congenital, type 2C, associated with acetylcholine receptor deficiency (CMS-2C)), OMIM:616314)

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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     
0000253869 (+) Pierre-Robin sequence,(+) Abnormality of eye movement,(+) Ptosis,(+) Muscular hypotonia,(+) Global developmental delay,(+) Bilateral ptosis,(+) Bradycardia,(+) Dysphagia,(+) Poor suck,(+) Apnea,(+) Upper airway obstruction - - Unknown 00y05m - - - - Andreas Laner 00335954
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