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Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II MeSH Supplementary Concept Data 2024


MeSH Supplementary
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II
Unique ID
C565531
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C565531
Entry Term(s)
CGD, Autosomal Recessive Cytochrome B-Positive, Type II
Granulomatous Disease, Chronic, due to NCF2 Deficiency
Neutrophil Cytosol Factor 2, Deficiency of
P67-Phox, Deficiency of
Registry Number
0
Heading Mapped to
*Granulomatous Disease, Chronic
NADPH Oxidases / *deficiency
Frequency
1
Note
mutation in NCF2
Date of Entry
2012/11/05
Revision Date
2013/11/06
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II Preferred
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