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Unexplained young onset end-stage renal disease - additional genes v0.121 SIX1 Achchuthan Shanmugasundram Phenotypes for gene: SIX1 were changed from Branchiootorenal Spectrum Disorders to Branchiootic syndrome 3, OMIM:608389; Deafness, autosomal dominant 23, OMIM:605192
Unexplained young onset end-stage renal disease - additional genes v0.68 SIX1 Achchuthan Shanmugasundram Added phenotypes Branchiootorenal Spectrum Disorders for gene: SIX1
Unexplained young onset end-stage renal disease - additional genes v0.65 SIX1 Achchuthan Shanmugasundram reviewed gene: SIX1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Unexplained young onset end-stage renal disease - additional genes v0.62 SIX1 Achchuthan Shanmugasundram Entity copied from Unexplained young onset end-stage renal disease v5.32
Unexplained young onset end-stage renal disease - additional genes v0.62 SIX1 Achchuthan Shanmugasundram gene: SIX1 was added
gene: SIX1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: SIX1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: SIX1 were set to Branchiootorenal Spectrum Disorders