FOXC2

forkhead box C2
OMIM: 602402, Gene2Phenotype

15 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 15 panels
Green FOXC2 in Eye Anterior Segment Abnormalities Level 2: Ophthalmological disorders Version 1.15	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Lymphedema-distichiasis syndrome 153400
Red FOXC2 in Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic Level 2: Renal and urinary tract disorders Version 0.159 Component of the following Super Panels: Congenital abnormalities of the kidneys and urinary tract (CAKUT)_SuperPanel Kidneyome_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Red Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus OMIM #153400
Red FOXC2 in Congenital diaphragmatic hernia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.17	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Lymphedema-distichiasis syndrome, MIM# 153400
Green FOXC2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.474	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green FOXC2 in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.328	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Lymphoedema-distichiasis syndrome, MIM:153400
Amber FOXC2 in Interstitial Lung Disease Level 2: Respiratory disorders Version 1.2	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus 153400 infant pulmonary lymphangiectasia
Green FOXC2 in Lymphoedema_nonsyndromic Level 2: Cardiovascular disorders Version 0.44 Component of the following Super Panels: Vascular Malformations SuperPanel	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green FOXC2 in Mendeliome Version 1.3512	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Lymphoedema-distichiasis syndrome, MIM# 153400
Green FOXC2 in Pierre Robin Sequence Level 2: Dysmorphic and congenital abnormality syndromes Version 0.53	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red FOXC2 in Monogenic Diabetes Level 2: Endocrine disorders Version 0.152 Component of the following Super Panels: Metabolic Disorders Superpanel	1 review	Unknown	Sources Radboud University Medical Center, Nijmegen Expert Review Red Phenotypes Lymphedema-distichiasis syndrome, 153400 Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus, 153400
Green FOXC2 in Lymphoedema_syndromic Level 3: Lymphatic Disorders Level 2: Cardiovascular disorders Version 0.12 Component of the following Super Panels: Vascular Malformations SuperPanel	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources London South GLH Expert Review Green UKGTN Eligibility statement prior genetic testing Radboud University Medical Center, Nijmegen Phenotypes Lymphedema-distichiasis syndrome, 153400 Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus, 153400
Green FOXC2 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Lymphoedema, primary
Green FOXC2 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Cleft palate LYMPHEDEMA-DISTICHIASIS SYNDROME
Green FOXC2 in Fetal anomalies Version 1.465	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Genomics England PanelApp Literature Phenotypes Lymphoedema-distichiasis syndrome, MIM# 153400
Red FOXC2 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category A gene Phenotypes Lymphoedema-distichiasis syndrome, MIM# 153400