HNF1B, HNF1 homeobox B, 6928

N. diseases: 279; N. variants: 72
Disease: Medullary cystic kidney disease 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1 		0.020 Biomarker disease BEFREE Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome. 16883323 2006
CUI: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1 		0.020 Biomarker disease BEFREE Identification and characterization of the MCKD and FJHN genes will help to clarify the pathogenesis and classification of hereditary tubulo-interstitial nephritides. 12832729 2003