C8A

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber C8A in Vasculitis Level 2: Immunological disorders Version 0.86	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes C8 deficiency, type I MIM#613790
Amber C8A in Mendeliome Version 1.2512	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes C8 deficiency, type I MIM#613790
Amber C8A in Complement Deficiencies Level 2: Immunological disorders Version 0.74 Component of the following Super Panels: Immunological disorders_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Melbourne Genomics Health Alliance Immunology Flagship Victorian Clinical Genetics Services Phenotypes C8 deficiency, type I MIM#613790
Red C8A in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.117	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BeginNGS Phenotypes C8 deficiency, type I, MIM# 613790

4 panels