AFP, alpha fetoprotein, 174

N. diseases: 392; N. variants: 9
Disease: Congenital absence of kidney ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney 		0.010 Biomarker disease BEFREE This case illustrates the potential severity of the renal anomalies in the BOR syndrome and the inadequacy of oligohydramnios and maternal serum alpha-fetoprotein as screening methods for renal agenesis. 6846397 1983