INTS11

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green INTS11 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities, MIM# 620428
Green INTS11 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities, MIM# 620428
Green INTS11 in Syndromic Retinopathy Level 2: Ophthalmological disorders Version 0.209 Component of the following Super Panels: Retinal Disorders Superpanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities, MIM# 620428

3 panels