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2013 MeSH

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Granulomatous Disease, Chronic
MeSH HeadingGranulomatous Disease, Chronic
Tree NumberC15.378.553.774.535
Tree NumberC16.320.322.233
Tree NumberC20.673.774.535
Annotationalso called granulomatous disease of childhood
Scope NoteA recessive X-linked defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation.
Allowable QualifiersBL CF CI CL CN CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Entry VersionGRANULOMATOUS DIS CHRONIC
Previous Indexing Granuloma (1966-1971)
Previous Indexing Immunologic Deficiency Syndromes (1968-1971)
Previous Indexing Phagocyte Bactericidal Dysfunction (1972-1977)
Previous Indexing Phagocytosis (1966-1971)
Online Notesearch PHAGOCYTE BACTERICIDAL DYSFUNCTION 1972-74
History Note78(75); was see under PHAGOCYTE BACTERICIDAL DYSFUNCTION 1972-77
Date of Entry19990101
Unique IDD006105


MeSH Tree Structures

 
Hemic and Lymphatic Diseases [C15]
   Hematologic Diseases [C15.378]
      Leukocyte Disorders [C15.378.553]
         Phagocyte Bactericidal Dysfunction [C15.378.553.774]
Chediak-Higashi Syndrome [C15.378.553.774.257]
Arrow pointing to current tree nodeGranulomatous Disease, Chronic [C15.378.553.774.535]
Job's Syndrome [C15.378.553.774.600]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Genetic Diseases, X-Linked [C16.320.322]
Aicardi Syndrome [C16.320.322.030]
Androgen-Insensitivity Syndrome [C16.320.322.061]
Barth Syndrome [C16.320.322.068]
Bulbo-Spinal Atrophy, X-Linked [C16.320.322.076]
Choroideremia [C16.320.322.092]
Dent Disease [C16.320.322.100]
Dyskeratosis Congenita [C16.320.322.108]
Ectodermal Dysplasia 1, Anhidrotic [C16.320.322.116]
Fabry Disease [C16.320.322.124]
Focal Dermal Hypoplasia [C16.320.322.186]
Glycogen Storage Disease Type IIb [C16.320.322.201]
Glycogen Storage Disease Type VIII [C16.320.322.217]
Arrow pointing to current tree nodeGranulomatous Disease, Chronic [C16.320.322.233]
Hemophilia B [C16.320.322.235]
Hyper-IgM Immunodeficiency Syndrome, Type 1 [C16.320.322.237]
Hypophosphatemic Rickets, X-Linked Dominant [C16.320.322.239]
Ichthyosis, X-Linked [C16.320.322.241]
Isolated Noncompaction of the Ventricular Myocardium [C16.320.322.370]
Mental Retardation, X-Linked [C16.320.322.500]  +
Muscular Dystrophy, Duchenne [C16.320.322.562]
Muscular Dystrophy, Emery-Dreifuss [C16.320.322.625]
Oculocerebrorenal Syndrome [C16.320.322.750]
Ornithine Carbamoyltransferase Deficiency Disease [C16.320.322.828]
Pelizaeus-Merzbacher Disease [C16.320.322.906]
Wiskott-Aldrich Syndrome [C16.320.322.937]
X-Linked Combined Immunodeficiency Diseases [C16.320.322.968]

 
Immune System Diseases [C20]
   Immunologic Deficiency Syndromes [C20.673]
      Phagocyte Bactericidal Dysfunction [C20.673.774]
Chediak-Higashi Syndrome [C20.673.774.257]  +
Arrow pointing to current tree nodeGranulomatous Disease, Chronic [C20.673.774.535]
Job's Syndrome [C20.673.774.600]

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