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Proteinuric renal disease v1.195 CYP11B2 Eleanor Williams Phenotypes for gene: CYP11B2 were changed from to Hypoaldosteronism, congenital, due to CMO I deficiency #203400; Hypoaldosteronism, congenital, due to CMO II deficiency #610600
Proteinuric renal disease v1.194 CYP11B2 Eleanor Williams Publications for gene: CYP11B2 were set to
Proteinuric renal disease v1.16 CYP11B2 Eleanor Williams reviewed gene: CYP11B2: Rating: RED; Mode of pathogenicity: ; Publications: PMID: 9814506, PMID: 24022297; Phenotypes: Hypoaldosteronism, congenital, due to CMO I deficiency #203400, Hypoaldosteronism, congenital, due to CMO II deficiency #610600; Mode of inheritance: Unknown; Current diagnostic: yes
Proteinuric renal disease v1.15 CYP11B2 Eleanor Williams Source NHS GMS was added to CYP11B2.