Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome b-Positive, Type I (*)

Alternative Names

CGD, Autosomal Recessive Cytochrome b-Positive, Type I
Granulomatous Disease, Chronic, due to NCF1 Deficiency
Neutrophil Cytosol Factor 1, Deficiency of
NCF1, Deficiency of
Soluble Oxidase Component II, Deficiency of
SOC2, Deficiency of
p47-PHOX, Deficiency of

WHO-ICD-10 version:2010

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

OMIM Number

233700

Mode of Inheritance

Autosomal recessive

Gene Map Locus

7q11.23

Table of content

Alternative Names
WHO ICD
OMIM Number
Mode of Inheritance
Edit History

Algeria
Bahrain
Comoros
Djibouti
Egypt
Eritrea
Iraq
Jordan
Kuwait
Lebanon
Libya
Mauritania
Morocco
Oman
Palestine
Qatar
Saudi Arabia
Somalia
Sudan
Syria
Tunisia
United Arab Emirates
Yemen

Countries with reported incidence
Countries without reported incidence
Non Arab countries

Edit History

Pratibha Nair: 19.01.2015

Notes

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CTGA Details

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome b-Positive, Type I (*)