SLC34A1, solute carrier family 34 member 1, 6569

N. diseases: 73; N. variants: 51
Disease: FANCONI RENOTUBULAR SYNDROME 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551503
Disease: FANCONI RENOTUBULAR SYNDROME 1
FANCONI RENOTUBULAR SYNDROME 1 		0.300 GermlineCausalMutation disease ORPHANET A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome. 20335586 2010