HOGA1

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green HOGA1 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hyperoxaluria, primary, type III MIM#613616
Red HOGA1 in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Hyperoxaluria, primary, type III (MIM#613616)
Green HOGA1 in Aminoacidopathy Level 2: Metabolic disorders Version 1.128 Component of the following Super Panels: Metabolic Disorders Superpanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes primary hyperoxaluria type 3 MONDO:0013327 Disorders of ornithine, proline and hydroxyproline metabolism
Green HOGA1 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Hyperoxaluria, primary, type III MIM#613616 Tags treatable metabolic
Green HOGA1 in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.14 Component of the following Super Panels: Kidneyome_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Expert Review Green KidGen_MetabolicRenal v38.1.0 Phenotypes Hyperoxaluria, primary, type III MIM#613616

5 panels