Phenotypes for disease #01688 (CANDF2 (candidiasis, familial, type 2 (CANDF-2)), OMIM:212050)

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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     
0000301662 best corrected visual acuity: 0.04; electroretinogram , rod: non- recordable, cone: severely reduced - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 53y - 38y - - LOVD 00409545
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