FOXE3

forkhead box E3
OMIM: 601094, ClinGen, DECIPHER

11 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 11 panels
Green FOXE3 in Anophthalmia_Microphthalmia_Coloboma Level 2: Ophthalmological disorders Version 1.43	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Anterior segment dysgenesis 2, multiple subtypes, MIM# 610256
Green FOXE3 in Eye Anterior Segment Abnormalities Level 2: Ophthalmological disorders Version 1.12	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Anterior segment dysgenesis 2, multiple subtypes, MIM# 610256
Amber FOXE3 in Aortopathy_Connective Tissue Disorders Level 2: Cardiovascular disorders Version 1.86	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes {Aortic aneurysm, familial thoracic 11, susceptibility to}, MIM# 617349
Amber FOXE3 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.52	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Aortic aneurysm, familial thoracic 11, susceptibility to, MIM# 617349
Green FOXE3 in Cataract Level 2: Ophthalmological disorders Version 0.373	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red FOXE3 in Corneal Dystrophy Level 2: Ophthalmological disorders Version 1.11	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Anterior segment dysgenesis 2, multiple subtypes, MIM# 610256
Amber FOXE3 in Glaucoma congenital Level 2: Ophthalmological disorders Version 1.9	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Expert list Phenotypes Anterior segment dysgenesis 2, multiple subtypes, MIM# 610256
Green FOXE3 in Mendeliome Version 1.2302	1 review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Anterior segment dysgenesis 2, multiple subtypes, MIM#610256 Cataract 34, multiple types, MIM#612968 Aortic aneurysm, familial thoracic 11, susceptibility to}, MIM#617349
Green FOXE3 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Aphakia, congenital primary, 610256 (3)
Green FOXE3 in Fetal anomalies Version 1.313	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Anterior segment dysgenesis 2, multiple subtypes, OMIM:610256 Cataract 34, multiple types, OMIM:612968
Green FOXE3 in Prepair 1000+ Level 2: Screening Version 1.1566	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Anterior segment dysgenesis 2, multiple subtypes, MIM# 610256