FBXW11

F-box and WD repeat domain containing 11
OMIM: 605651, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green FBXW11 in Anophthalmia_Microphthalmia_Coloboma Level 2: Ophthalmological disorders Version 1.50	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Literature Phenotypes Neurodevelopmental, eye, jaw, and digital syndrome (NDEJD), MIM#618914 Intellectual disability developmental eye anomalies digital anomalies
Green FBXW11 in Mendeliome Version 1.3512	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Literature Phenotypes Neurodevelopmental, eye, jaw, and digital syndrome (NDEJD), MIM#618914 Intellectual disability developmental eye anomalies digital anomalies
Red FBXW11 in Autoinflammatory Disorders Level 2: Immunological disorders Version 2.28 Component of the following Super Panels: Immunological disorders_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Autoinflammatory disorder MONDO:0019751, FBXW11-related
Green FBXW11 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Literature Phenotypes Neurodevelopmental, eye, jaw, and digital syndrome (NDEJD), MIM#618914 Intellectual disability developmental eye anomalies digital anomalies
Green FBXW11 in Fetal anomalies Version 1.465	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Neurodevelopmental, eye, jaw, and digital syndrome (NDEJD), MIM#618914