ERCC3:Ensemblv90

Panel	Reviews	Mode of inheritance	Details
Filter panels 33 panels
Red ERCC3 in Brain Calcification Level 2: Neurology and neurodevelopmental disorders Version 2.0 Component of the following Super Panels: Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes Xeroderma pigmentosum, group B, MIM# 610651
Green ERCC3 in Cataract Level 2: Ophthalmological disorders Version 0.396	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green ERCC3 in Chromosome Breakage Disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 1.24	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651
Red ERCC3 in Ichthyosis and Porokeratosis Level 2: Dermatological disorders Version 1.23	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Trichothiodystrophy 2, photosensitive MIM#616390
Green ERCC3 in Mendeliome Version 1.3802	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651
Green ERCC3 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.132	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green ERCC3 in Photosensitivity Syndromes Level 2: Dysmorphic and congenital abnormality syndromes Version 1.11	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651
Green ERCC3 in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.601	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green ERCC3 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.304	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Xeroderma pigmentosum, group B 61, MIM#0651
Red ERCC3 in Hyper-IgE syndrome Level 2: Immunological disorders Version 1.6	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Melbourne Genomics Health Alliance Immunology Flagship Victorian Clinical Genetics Services Australian Genomics Health Alliance Immunology Flagship Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651
Green ERCC3 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes xeroderma pigmentosum group B MONDO:0012531
Red ERCC3 in Leukodystrophy - paediatric Level 2: Neurology and neurodevelopmental disorders Version 0.334 Component of the following Super Panels: Leukodystrophy_Superpanel Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Phenotypes Trichothiodystrophy 2, photosensitive 616390
Red ERCC3 in CGC_86 Version 0.3	0 reviews	Other	Sources CGC_86 Phenotypes Xeroderma Pigmentosum, Complementation Group B
Red ERCC3 in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes Xeroderma Pigmentosum, Complementation Group B
Red ERCC3 in TCGA_PANCAN_2018 Version 0.3	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Xeroderma Pigmentosum, Complementation Group B
Green ERCC3 in Hair disorders Level 2: Dermatological disorders Version 0.81	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Green Literature Victorian Clinical Genetics Services Phenotypes Trichothiodystrophy 2, photosensitive, 616390
Red ERCC3 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category C gene Phenotypes Xeroderma pigmentosum
Green ERCC3 in Growth failure Version 1.87	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651
Green ERCC3 in Fetal anomalies Version 1.482	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Xeroderma pigmentosum, group B 61, MIM#0651 Trichothiodystrophy 2, photosensitive, MIM# 616390
Red ERCC3 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.141	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category C gene Expert Review Red Phenotypes Xeroderma pigmentosum
Red ERCC3 in Brain Calcification Level 2: Neurology and neurodevelopmental disorders Version 3.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Red Phenotypes Xeroderma pigmentosum, group B, MIM# 610651
Green ERCC3 in Cataract Level 2: Ophthalmological disorders Version 1.0	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services
Green ERCC3 in Chromosome Breakage Disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651
Red ERCC3 in Ichthyosis and Porokeratosis Level 2: Dermatological disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Literature Expert Review Red Phenotypes Trichothiodystrophy 2, photosensitive MIM#616390
Green ERCC3 in Cancer Predisposition_Paediatric Level 2: Cancer Version 1.0	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services
Green ERCC3 in Photosensitivity Syndromes Level 2: Dysmorphic and congenital abnormality syndromes Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Victorian Clinical Genetics Services Expert Review Green Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651
Green ERCC3 in Regression Level 2: Neurology and neurodevelopmental disorders Version 1.0	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services
Green ERCC3 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 2.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Victorian Clinical Genetics Services Expert Review Green Phenotypes Xeroderma pigmentosum, group B 61, MIM#0651
Red ERCC3 in Hyper-IgE syndrome Level 2: Immunological disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Immunology Flagship Victorian Clinical Genetics Services Melbourne Genomics Health Alliance Immunology Flagship Expert Review Red Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651
Green ERCC3 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Genetic Health Queensland Expert Review Green Phenotypes xeroderma pigmentosum group B MONDO:0012531
Red ERCC3 in Leukodystrophy - paediatric Level 2: Neurology and neurodevelopmental disorders Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Phenotypes Trichothiodystrophy 2, photosensitive 616390
Red ERCC3 in TCGA_PANCAN_2018 Version 1.0	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Xeroderma Pigmentosum, Complementation Group B
Green ERCC3 in Growth failure Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Expert Review Green Phenotypes Trichothiodystrophy 2, photosensitive, MIM# 616390 Xeroderma pigmentosum, group B 61, MIM#0651

ERCC3:Ensemblv90

33 panels

Red ERCC3 in Brain Calcification

Sources

Phenotypes

Green ERCC3 in Cataract

Sources

Green ERCC3 in Chromosome Breakage Disorders

Sources

Phenotypes

Red ERCC3 in Ichthyosis and Porokeratosis

Sources

Phenotypes

Green ERCC3 in Mendeliome

Sources

Phenotypes

Green ERCC3 in Cancer Predisposition_Paediatric

Sources

Green ERCC3 in Photosensitivity Syndromes

Sources

Phenotypes

Green ERCC3 in Regression

Sources

Green ERCC3 in Deafness_IsolatedAndComplex

Sources

Phenotypes

Red ERCC3 in Hyper-IgE syndrome

Sources

Phenotypes

Green ERCC3 in Intellectual disability syndromic and non-syndromic

Sources

Phenotypes

Red ERCC3 in Leukodystrophy - paediatric

Sources

Phenotypes

Red ERCC3 in CGC_86

Sources

Phenotypes

Red ERCC3 in NCGC

Sources

Phenotypes

Red ERCC3 in TCGA_PANCAN_2018

Sources

Phenotypes

Green ERCC3 in Hair disorders

Sources

Phenotypes

Red ERCC3 in Additional findings_Paediatric

Sources

Phenotypes

Green ERCC3 in Growth failure

Sources

Phenotypes

Green ERCC3 in Fetal anomalies

Sources

Phenotypes

Red ERCC3 in Genomic newborn screening: BabyScreen+

Sources

Phenotypes

Red ERCC3 in Brain Calcification

Sources

Phenotypes

Green ERCC3 in Cataract

Sources

Green ERCC3 in Chromosome Breakage Disorders

Sources

Phenotypes

Red ERCC3 in Ichthyosis and Porokeratosis

Sources

Phenotypes

Green ERCC3 in Cancer Predisposition_Paediatric

Sources

Green ERCC3 in Photosensitivity Syndromes

Sources

Phenotypes

Green ERCC3 in Regression

Sources

Green ERCC3 in Deafness_IsolatedAndComplex

Sources

Phenotypes