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- B6142c112e4e1bb01ffd22b0bc314b87c NCIT_P378 "NCI" @default.
- B6142c112e4e1bb01ffd22b0bc314b87c type Axiom @default.
- B6142c112e4e1bb01ffd22b0bc314b87c annotatedProperty IAO_0000115 @default.
- B6142c112e4e1bb01ffd22b0bc314b87c annotatedSource NCIT_C128145 @default.
- B6142c112e4e1bb01ffd22b0bc314b87c 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.