APOA2

Panel	Reviews	Mode of inheritance	Details
Red APOA2 in Vasculitis Level 2: Immunological disorders Version 0.82	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Apolipoprotein A-II deficiency {Hypercholesterolemia, familial, modifier of} MIM#143890
Red APOA2 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Apolipoprotein A-II deficiency {Hypercholesterolemia, familial, modifier of} MIM#143890

Panel

Reviews

Mode of inheritance

Details

Level 2: Immunological disorders
Version 0.82

review

BIALLELIC, autosomal or pseudoautosomal

Version 1.1902

review

BIALLELIC, autosomal or pseudoautosomal

2 panels