Human Disease and Mouse Model Detail
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Human Disease
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Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II
OMIM ID: 233710
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Synonyms
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Cgd, Autosomal Recessive Cytochrome B-Positive, Type II;
Granulomatous Disease, Chronic, Due to NCF2 Deficiency;
Ncf2, Deficiency of;
Neutrophil Cytosol Factor 2, Deficiency of;
P67-Phox, Deficiency of
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Ncf2
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NCF2*
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1:1 Homology
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Analysis Tools