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Granulomatous Disease, Chronic MeSH Descriptor Data 2023


MeSH Heading
Granulomatous Disease, Chronic
Tree Number(s)
C15.378.553.774.535
C16.320.322.233
C20.673.774.535
C23.550.291.500.423
Unique ID
D006105
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006105
Annotation
also called granulomatous disease of childhood
Scope Note
A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation. When chronic granulomatous disease is caused by mutations in the CYBB gene, the condition is inherited in an X-linked recessive pattern. When chronic granulomatous disease is caused by CYBA, NCF1, NCF2, or NCF4 gene mutations, the condition is inherited in an autosomal recessive pattern.
Entry Version
GRANULOMATOUS DIS CHRONIC
Entry Term(s)
Autosomal Recessive Chronic Granulomatous Disease
Chronic Granulomatous Disease
Chronic Granulomatous Disease, Atypical
Chronic Granulomatous Disease, X-Linked
Cytochrome B-Negative Granulomatous Disease, Chronic, X-Linked
Cytochrome B-Positive Granulomatous Disease, Chronic, X-Linked
Granulomatous Disease, Chronic, X-Linked
Granulomatous Disease, Chronic, X-Linked, Variant
X-Linked Chronic Granulomatous Disease
NLM Classification #
QW 740
Previous Indexing
Granuloma (1966-1971)
Immunologic Deficiency Syndromes (1968-1971)
Phagocyte Bactericidal Dysfunction (1972-1977)
Phagocytosis (1966-1971)
Public MeSH Note
78; was see under PHAGOCYTE BACTERICIDAL DYSFUNCTION 1972-77
Online Note
search PHAGOCYTE BACTERICIDAL DYSFUNCTION 1972-74
History Note
78(75); was see under PHAGOCYTE BACTERICIDAL DYSFUNCTION 1972-77
Date Established
1978/01/01
Date of Entry
1999/01/01
Revision Date
2021/03/12
Granulomatous Disease, Chronic Preferred
Autosomal Recessive Chronic Granulomatous Disease Narrower
Granulomatous Disease, Chronic, X-Linked Broader
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