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21 Possible Causes for Autosomal Recessive Cytochrome B-Positive CGD Type 1

  • 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]

  • Chronic Granulomatous Disease

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

  • Laron Syndrome with Immunodeficiency

    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] 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]

  • Autoimmune Lymphoproliferative Syndrome Type 3

    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] 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]

  • Autosomal Agammaglobulinemia

    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] 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]

  • Primary CD59 Deficiency

    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] 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]

  • Lymphedema Hypoparathyroidism Syndrome

    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] 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]

  • 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]

  • 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]

  • Combined Immunodeficiency due to CD3-Gamma Deficiency

    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] 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]

Further symptoms