Phenotypes for disease #01686 (PFIC1 (cholestasis, intrahepatic, familial, progressive, type 1 (PFIC-1)), OMIM:211600)

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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     
0000301660 best corrected visual acuity: 0.7; electroretinogram , rod: severely reduced, cone: mildly reduced - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 56y - 40y - - LOVD 00409543
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