Phenotypes for disease #01028 (MKKS (McKusick-Kaufman syndrome (MKKS)), OMIM:236700)

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Individual ID     
0000309919 - - McKusick-Kaufman syndrome Familial, autosomal recessive - - - - - LOVD 00418583
0000309920 hydrometrocolpos surgically repaired on the first day of life; postaxial polydactyly of one hand and both feet; an atrioventricular septal defect without significant shunting diagnosed originally by fetal echocardiography;other abnormalities noted at birth: hypoplastic clitoris with prominent labia majora, cystic dysplasia of the kidneys with mild hydronephrosis and small ears - McKusick-Kaufman syndrome Familial, autosomal recessive - - - - - LOVD 00418584
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