IGBP1, immunoglobulin binding protein 1, 3476

N. diseases: 57; N. variants: 0
Disease: Alport Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome 		0.010 GeneticVariation disease BEFREE Previous studies have indicated that mutation of type IV collagen alpha4 gene may be responsible for both BFH and AS. 14524583 2003