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Unexplained young onset end-stage renal disease - additional genes v0.111 ACTA2 Achchuthan Shanmugasundram Phenotypes for gene: ACTA2 were changed from Multi system smooth muscle dysfunction to Smooth muscle dysfunction syndrome, OMIM:613834
Unexplained young onset end-stage renal disease - additional genes v0.68 ACTA2 Achchuthan Shanmugasundram Added phenotypes Multi system smooth muscle dysfunction for gene: ACTA2
Unexplained young onset end-stage renal disease - additional genes v0.65 ACTA2 Achchuthan Shanmugasundram reviewed gene: ACTA2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease - additional genes v0.39 ACTA2 Achchuthan Shanmugasundram Entity copied from Unexplained young onset end-stage renal disease v5.32
Unexplained young onset end-stage renal disease - additional genes v0.39 ACTA2 Achchuthan Shanmugasundram gene: ACTA2 was added
gene: ACTA2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: ACTA2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: ACTA2 were set to Multi system smooth muscle dysfunction