Phenotypes for disease #01689 (CDG1A (glycosylation, congenital disorder of, type Ia (CDG-1A)), OMIM:212065)

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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     
0000301663 best corrected visual acuity: 0.5; electroretinogram , rod: severely reduced, cone: severely reduced - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 65y - 26y - - LOVD 00409546
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