MeSH Browser

MeSH Supplementary: Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I
Unique ID: C565532
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565532
Entry Term(s): CGD, Autosomal Recessive Cytochrome B-Positive, Type I; Granulomatous Disease, Chronic, due to NCF1 Deficiency; Neutrophil Cytosol Factor 1, Deficiency of; P47-Phox, Deficiency of; Soluble Oxidase Component II, Deficiency of
Registry Number: 0
Heading Mapped to: *Granulomatous Disease, Chronic; NADPH Oxidases / *deficiency
Frequency: 5
Note: mutation in NCF1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

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