SERPINA4, serpin family A member 4, 5267

N. diseases: 45; N. variants: 3
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 GeneticVariation disease BEFREE In addition, the high frequency of unilateral renal aplasia in X-linked Kallmann patients (6 out of 11 males with identified alterations of the KAL gene) should be emphasized. 8504298 1993