SLC34A1, solute carrier family 34 member 1, 6569

N. diseases: 73; N. variants: 51
Disease: FANCONI RENOTUBULAR SYNDROME 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3150652
Disease: FANCONI RENOTUBULAR SYNDROME 2
FANCONI RENOTUBULAR SYNDROME 2 		0.300 Biomarker disease GENOMICS_ENGLAND A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome. 20335586 2010