Phenotypes for disease #01696 (ODRMD (optic disc anomalies with retinal and/or macular dystrophy (ODRMD)), OMIM:212550)

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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     
0000301670 best corrected visual acuity: 1.2; electroretinogram , rod: mildly reduced, cone: mildly reduced - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 53y - - - - LOVD 00409553
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