Autosomal Recessive Cytochrome B-Positive CGD Type 1 Causes & Reasons

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Autosomal Recessive Cytochrome B-Positive CGD Type 1 Symptom Checker: Possible causes include Chronic Granulomatous Disease due to NCF2 Deficiency. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search.

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Possible Causes

Chronic Granulomatous Disease due to NCF2 Deficiency

recessive cytochrome b-negative CGD CYBA: mutations of CYBA in autosomal recessive cytochrome b-negative CGD (MIM.233690) cytochrome b-positive CGD -* NCF1 (7q11.23): autosomal [humpath.com]

Recessive, Cytochrome B-Positive, Type I CGD, Autosomal Recessive Cytochrome B-Positive, Type I Granulomatous Disease, Chronic, Due To NCF1 Deficiency NCF1, Deficiency Of [ukgtn.nhs.uk]

CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-POSITIVE, TYPE II; GRANULOMATOUS DISEASE, CHRONIC, DUE TO NCF2 DEFICIENCY; NCF2, DEFICIENCY OF; NEUTROPHIL CYTOSOL FACTOR 2, DEFICIENCY [rgd.mcw.edu]

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Chronic Granulomatous Disease

There are several types, including:[18] X-linked chronic granulomatous disease (CGD) autosomal recessive cytochrome b-negative CGD autosomal recessive cytochrome b-positive [en.wikipedia.org]

Autosomal recessive cytochrome b-positive CGD type I. There is mutation at gene locus 7q11.23 [ 4 ]. The type II has mutation at gene locus 1q25 [ 5 ]. [patient.info]

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Laron Syndrome with Immunodeficiency

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Autoimmune Lymphoproliferative Syndrome Type 3

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Autosomal Agammaglobulinemia

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Primary CD59 Deficiency

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Lymphedema Hypoparathyroidism Syndrome

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Combined Immunodeficiency due to CD3-Gamma Deficiency

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Pediatric Chronic Granulomatous Disease

There are several types, including: [17] X-linked chronic granulomatous disease (CGD) autosomal recessive cytochrome b-negative CGD autosomal recessive cytochrome b-positive [en.wikipedia.org]

CGD type I autosomal recessive cytochrome b-positive CGD type II atypical granulomatous disease Treatment [ edit ] Management of chronic granulomatous disease revolves around [en.wikipedia.org]

[…] two goals: 1) diagnose the disease early so that antibiotic prophylaxis can be given to keep an infection from occurring, and 2) educate the patient about his or her condition [en.wikipedia.org]

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Granulomatous Liver Disease

Autosomal recessive cytochrome b-positive CGD type I. There is mutation at gene locus 7q11.23 [ 4 ]. The type II has mutation at gene locus 1q25 [ 5 ]. [patient.info]

recessive CGD (AR-CGD), and mutation of CYBB causes X-linked CGD [ 1 ]. [patient.info]

[…] caused by pathogenic variants in one of five genes that encode the subunits of phagocyte NADPH oxidase: biallelic pathogenic variants in CYBA, NCF1, NCF2 and NCF4 cause autosomal [patient.info]

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Neonatal Inflammatory Skin and Bowel Disease

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Common Variable Immunodeficiency Type 8 with Autoimmunity

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Neonatal Inflammatory Skin and Bowel Disease 2

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Autosomal Recessive Agammaglobulinemia

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Autosomal Recessive Agammaglobulinemia Type 3

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Autosomal Recessive Monocyte and Dendritic Cell Deficiency

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Autosomal Recessive Agammaglobulinemia Type 4

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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T-B+ Severe Combined Immunodeficiency due to CD3zeta

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Tyrosine Kinase 2 Deficiency

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Spondylometaphyseal Dysplasia with Combined Immunodeficiency

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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Complement Component 8 Deficiency Type 1

Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II CGD, Autosomal Recessive Cytochrome B-Positive, Type II Granulomatous Disease, Chronic, Due To NCF2 [ukgtn.nhs.uk]

Neutrophil Cytosol Factor 1, Deficiency Of p47-PHOX, Deficiency Of SOC2, Deficiency Of Soluble Oxidase Component II, Deficiency Of 233700 Genetic Test Registry Granulomatous [ukgtn.nhs.uk]

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