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Refine by Category 46,XY sex reversal 8 2 Hyperbilirubinemia, Rotor type 2 Essential hypertension 1 Familial hypercholanemia 1 Alpha-methylacyl-CoA racemase deficiency 1 Hyperthyroxinemia, familial dysalbuminemic 1 Analbuminemia 1 Leukoencephalopathy with dystonia and motor neuropathy 1 Cerebrotendinous xanthomatosis 1 Perrault syndrome 1 1 Cholestasis, benign recurrent intrahepatic, 2 1 Primary bile acid malabsorption 1 Cholestasis, progressive familial intrahepatic, 2 1 Spastic paraplegia 5A, autosomal recessive 1 Cholestasis, progressive familial intrahepatic, 5 1 Congenital bile acid synthesis defect 1 1 Congenital bile acid synthesis defect 2 1 Congenital bile acid synthesis defect 3 1 Congenital bile acid synthesis defect 4 1 Congenital bile acid synthesis defect 6 1
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