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Complement Deficiencies v0.72 C8A Zornitza Stark Marked gene: C8A as ready
Complement Deficiencies v0.72 C8A Zornitza Stark Gene: c8a has been classified as Amber List (Moderate Evidence).
Complement Deficiencies v0.72 C8A Zornitza Stark Phenotypes for gene: C8A were changed from to C8 deficiency, type I MIM#613790
Complement Deficiencies v0.71 C8A Zornitza Stark Publications for gene: C8A were set to
Complement Deficiencies v0.70 C8A Zornitza Stark Mode of inheritance for gene: C8A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Complement Deficiencies v0.69 C8A Zornitza Stark Classified gene: C8A as Amber List (moderate evidence)
Complement Deficiencies v0.69 C8A Zornitza Stark Gene: c8a has been classified as Amber List (Moderate Evidence).
Complement Deficiencies v0.68 C8A Zornitza Stark reviewed gene: C8A: Rating: AMBER; Mode of pathogenicity: None; Publications: 9759902, 32769119; Phenotypes: C8 deficiency, type I MIM#613790; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Complement Deficiencies v0.0 C8A Zornitza Stark gene: C8A was added
gene: C8A was added to Complement deficiencies_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship
Mode of inheritance for gene: C8A was set to Unknown