Granulomatous Disease, Chronic, Autosomal Recessive, 2 (CGD2)

Alias:

Chronic Granulomatous Disease Due to Deficiency of Ncf-2

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type 2

Autosomal Recessive Chronic Granulomatous Disease Cytochrome B-Positive Type Ii

P67-Phox Deficiency

Ncf2 Deficiency

Cgd2

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

Chronic Granulomatous Disease Autosomal Recessive Cytochrome B-Positive Type Ii

Granulomatous Disease, Chronic, Due to Deficiency of Ncf-2, Type 2

Cgd, Autosomal Recessive Cytochrome B-Positive, Type Ii

Granulomatous Disease, Chronic, Due to Ncf2 Deficiency

Chronic Granulomatous Disease 2, Autosomal Recessive

Autosomal Recessive Chronic Granulomatous Disease 2

Deficiency of Neutrophil Cytosol Factor 2

Neutrophil Cytosol Factor 2 Deficiency

Avellino Corneal Dystrophy

Deficiency of P67-Phox

Deficiency of Ncf2

Cdg2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Granulomatous Disease, Chronic, Autosomal Recessive, 2, also known as chronic granulomatous disease due to deficiency of ncf-2, is related to corneal dystrophy, avellino type and suppurative lymphadenitis, and has symptoms including glare - eye symptom An important gene associated with Granulomatous Disease, Chronic, Autosomal Recessive, 2 is NCF2 (Neutrophil Cytosolic Factor 2), and among its related pathways/superpathways are Glycosylation and related congenital defects and Detoxification of Reactive Oxygen Species. Affiliated tissues include neutrophil and bone marrow, and related phenotypes are splenomegaly and hepatomegaly

Related ID：

MALACARDS：GRN063

OMIM：233710

MESH：D006105