Granulomatous Disease, Chronic, Autosomal Recessive, 1 (CGD1)

Alias:

Chronic Granulomatous Disease Due to Deficiency of Ncf-1

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type 1

Autosomal Recessive Chronic Granulomatous Disease Cytochrome B-Positive Type I

Deficiency of Neutrophil Cytosol Factor 1

Soluble Oxidase Component Ii Deficiency

P47-Phox Deficiency

Ncf1 Deficiency

Soc2 Deficiency

Cgd1

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I

Chronic Granulomatous Disease Autosomal Recessive Cytochrome B-Positive Type I

Granulomatous Disease, Chronic, Due to Deficiency of Ncf-1, Type 1

Cgd, Autosomal Recessive Cytochrome B-Positive, Type I

Granulomatous Disease, Chronic, Due to Ncf1 Deficiency

Chronic Granulomatous Disease 1, Autosomal Recessive

Chronic Granulomatous Disease Due to Ncf1 Deficiency

Autosomal Recessive Chronic Granulomatous Disease 1

Deficiency of Soluble Oxidase Component Ii

Neutrophil Cytosol Factor 1 Deficiency

Deficiency of P47-Phox

Deficiency of Ncf1

Deficiency of Soc2

Cdg1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Granulomatous Disease, Chronic, Autosomal Recessive, 1, also known as chronic granulomatous disease due to deficiency of ncf-1, is related to chronic granulomatous disease and muscular dystrophy-dystroglycanopathy , type c, 15. An important gene associated with Granulomatous Disease, Chronic, Autosomal Recessive, 1 is NCF1 (Neutrophil Cytosolic Factor 1), and among its related pathways/superpathways are Signal Transduction and Signaling by Rho GTPases. Affiliated tissues include neutrophil and bone marrow, and related phenotypes are impaired oxidative burst and splenomegaly

Related ID：

MALACARDS：GRN062

OMIM：233700

MESH：D006105