agammaglobulinemia

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Information
Disease name
agammaglobulinemia
Disease ID
DOID:2583
Description
"A B cell deficiency that is caused by a reduction in all types of gamma globulins." [url:http\://en.wikipedia.org/wiki/Dysgammaglobulinemia]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT00161993 Completed Phase 2 Safety, Pharmacokinetic and Efficacy Study of a 10% Triple Virally Reduced Intravenous Immune Globulin Solution in Patients With Primary Immunodeficiency (Hypo- or Agammaglobulinemia) June 13, 2002 September 24, 2003
NCT00168012 Completed Phase 3 Efficacy and Safety of Intravenous Immunoglobulin IVIG-F10 in Patients With Primary Immunodeficiencies (PID) September 2004 September 2005
NCT00168025 Completed Phase 3 Efficacy and Safety of Intravenous Immunoglobulin IgPro10 in Patients With Primary Immunodeficiencies (PID) September 2004 March 2006
NCT00220766 Completed Phase 3 Rapid Infusion of Immune Globulin Intravenous (Human) In Primary Immunodeficiency Patients August 2002 March 2004
NCT00322556 Completed Phase 3 Safety and Efficacy of Intravenous Immunoglobulin IgPro10 in Patients With Primary Immunodeficiencies (PID) November 2005 April 2008
NCT00520494 Completed Phase 4 Efficacy and Safety of Vivaglobin® in Previously Untreated Patients With Primary Immunodeficiency March 2007 October 2008
NCT00661401 Completed N/A Specific IgG Antibody in Patients With Primary Antibody Deficiencies Treated With Subcutaneous Immunoglobulin January 2002 November 2002
NCT01581593 Completed Phase 3 Efficacy and Safety Study of Kedrion IVIG 10% to Treat Subjects With Primary Immunodeficiency (PID) November 12, 2012 August 27, 2014
Disase is a (Disease Ontology)
DOID:2115
Cross Reference ID (Disease Ontology)
ICD10CM:D80.1
Cross Reference ID (Disease Ontology)
ICD9CM:279.00
Cross Reference ID (Disease Ontology)
MESH:D000361
Cross Reference ID (Disease Ontology)
MIM:PS601495
Cross Reference ID (Disease Ontology)
NCI:C26931
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:119250001
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:267512002
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0001768
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0086438
Exact Synonym (Disease Ontology)
hypogammaglobulinemia
Exact Synonym (Disease Ontology)
IGHM
Exact Synonym (Disease Ontology)
mu heavy chain deficiency
HPO alt_id (Human Phenotype Ontology)
HP:0008328
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0004432
OMIM Phenotype Series Number (OMIM)
PS601495
MeSH unique ID (MeSH (Medical Subject Headings))
D000361