MeSH Browser

MeSH Supplementary: Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
Unique ID: C565533
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565533
Entry Term(s): CYBA Deficiency; Chronic Granulomatous Disease due to Deficiency of the Alpha Subunit of Cytochrome B; Chronic Granulomatous Disease, Autosomal Recessive Cytochrome B-Negative
Registry Number: 0
Heading Mapped to: *Granulomatous Disease, Chronic; NADPH Oxidases / *deficiency
Frequency: 5
Note: mutation in CYBA
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative MeSH Supplementary Concept Data 2024