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
Exact Synonym (Disease Ontology)
hypogammaglobulinemia
Exact Synonym (Disease Ontology)
IGHM
Exact Synonym (Disease Ontology)
mu heavy chain deficiency
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
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0004432
HPO alt_id (Human Phenotype Ontology)
HP:0008328
OMIM Phenotype Series Number (OMIM)
PS601495
MeSH unique ID (MeSH (Medical Subject Headings))
D000361