| Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.300 | Biomarker | phenotype | RGD | A missense LAMB2 mutation causes congenital nephrotic syndrome by impairing laminin secretion. | 21511833 | 2011 | ||||
|
0.300 | Biomarker | phenotype | HPO |