UBE2U

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Red UBE2U in Cataract Level 2: Ophthalmological disorders Version 0.375	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Retinoschisis cataracts learning disabilities developmental delay
Red UBE2U in Mendeliome Version 1.3512	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Retinoschisis cataracts learning disabilities developmental delay
Red UBE2U in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Retinoschisis cataracts learning disabilities developmental delay

3 panels