C1QTNF5

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green C1QTNF5 in Mendeliome Version 1.1902	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Retinal degeneration, late-onset, autosomal dominant MIM#605670
Green C1QTNF5 in Retinitis pigmentosa_Autosomal Dominant Level 2: Ophthalmological disorders Version 0.57 Component of the following Super Panels: Retinal Disorders Superpanel Retinitis Pigmentosa Superpanel	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Retinal degeneration, late-onset, autosomal dominant MIM#605670
Green C1QTNF5 in Macular Dystrophy/Stargardt Disease Level 2: Ophthalmological disorders Version 0.45 Component of the following Super Panels: Retinal Disorders Superpanel	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Royal Melbourne Hospital Expert Review Green Phenotypes Retinal degeneration, late-onset, autosomal dominant, 605670 Retinitis pigmentosa

3 panels