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- B5adb1a303045be1cb01b08de8d9e5a5d NCIT_P378 "NICHD" @default.
- B5adb1a303045be1cb01b08de8d9e5a5d type Axiom @default.
- B5adb1a303045be1cb01b08de8d9e5a5d annotatedProperty NCIT_P325 @default.
- B5adb1a303045be1cb01b08de8d9e5a5d annotatedSource NCIT_C128145 @default.
- B5adb1a303045be1cb01b08de8d9e5a5d annotatedTarget "An autosomal recessive disorder caused by mutation(s) in the LAMB2 gene, encoding laminin subunit beta-2. It is characterized by congenital nephrotic syndrome with diffuse mesangial sclerosis and distinct ocular abnormalities." @default.