NR2F2

nuclear receptor subfamily 2 group F member 2
OMIM: 107773, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green NR2F2 in Congenital diaphragmatic hernia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.14	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Congenital heart defects, multiple types, 4, MIM# 615779
Green NR2F2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.418	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes 46,XX sex reversal 5 - MIM#618901 Congenital heart defects, multiple types, 4 - MIM#615779
Green NR2F2 in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 0.293	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes 46XX sex reversal 5, MIM# 618901
Green NR2F2 in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Krithika Murali (Victorian Clinical Genetics Services) 46,XX sex reversal 5 - MIM#618901 Congenital heart defects, multiple types, 4 - MIM#615779 Current 46,XX sex reversal 5 - MIM#618901 Congenital heart defects, multiple types, 4 - MIM#615779 Edit 46,XX sex reversal 5 - MIM#618901 Congenital heart defects, multiple types, 4 - MIM#615779
Green NR2F2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Syndromic disease, MONDO:0002254, NR2F2-related
Green NR2F2 in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Expert list Literature Phenotypes Congenital heart defects, multiple types, 4, MIM# 615779