Phenotypes for disease #01690 (CDG2A (glycosylation, congenital disorder of, type IIa (CDG-2A)), OMIM:212066)

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000301664 best corrected visual acuity: 0.6; electroretinogram , rod: mildly reduced, cone: severely reduced - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 64y - - - - LOVD 00409547
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.