NCF2

neutrophil cytosolic factor 2
OMIM: 608515, Gene2Phenotype

11 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 11 panels
Green NCF2 in Vasculitis Level 2: Immunological disorders Version 0.82	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Chronic granulomatous disease 2, autosomal recessive, MIM# 233710
Red NCF2 in Cataract Level 2: Ophthalmological disorders Version 0.366	review	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services
Green NCF2 in Inflammatory bowel disease Level 2: Gastroenterological disorders Version 0.121 Component of the following Super Panels: Immunological disorders_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Chronic granulomatous disease 2, autosomal recessive, MIM# 233710
Green NCF2 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Chronic granulomatous disease 2, autosomal recessive, MIM# 233710
Green NCF2 in Phagocyte Defects Level 2: Immunological disorders Version 1.29 Component of the following Super Panels: Immunological disorders_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Melbourne Genomics Health Alliance Immunology Flagship Victorian Clinical Genetics Services Phenotypes Chronic granulomatous disease 2, autosomal recessive, MIM# 233710
Green NCF2 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Chronic granulomatous disease due to deficiency of NCF-2, 233710 (3)
Green NCF2 in Chronic granulomatous disease Level 2: Immunological disorders Version 1.3	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Chronic granulomatous disease due to deficiency of NCF-2 MIM#233710
Green NCF2 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Chronic granulomatous disease
Green NCF2 in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Chronic granulomatous disease due to deficiency of NCF-2, 233710 (3)
Green NCF2 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene BeginNGS Phenotypes Chronic granulomatous disease, MIM#233710 Tags treatable immunological
Green NCF2 in Prepair 500+ Level 2: Screening Version 1.1	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Chronic granulomatous disease due to deficiency of NCF-2, 233710 (3)