Agammaglobulinemia

Symptom Information:

Symptom ID: HPO:0004432
Synonyms:
Agammaglobulinaemia [HPO:0004432]
Agammaglobulinemia (finding) [Orphanet:47160]
Agammaglobulinemia [Orphanet:47160]
Agammaglobulinemia [OMIM:Agammaglobulinemia]
Agammaglobulinemia/hypogammaglobulinemia/B-cell deficiency [Orphanet:47160]
Hypogammaglobulinaemia [MedDRA:10020983]
Agammaglobulinaemia [MedDRA:10020983]
Agammaglobulinemia [MedDRA:10020983]
Hypogammaglobulinaemia NOS [MedDRA:10020983]
Hypogammaglobulinemia, unspecified [MedDRA:10020983]
Other selective immunoglobulin deficiencies [MedDRA:10020983]
Physiologic hypogammaglobulinemia [MedDRA:10020983]
Hypogammaglobulinemia [MedDRA:10020983]
Hypogammaglobulinaemia, unspecified [MedDRA:10020983]
Physiologic hypogammaglobulinaemia [MedDRA:10020983]
Panhypogammaglobulinaemia [MedDRA:10020983]
Panhypogammaglobulinemia [MedDRA:10020983]
Hypogammaglobulinemia (1 patient) [OMIM:Hypogammaglobulinemia (1 patient)]
Humoral immune defect [MedDRA:10020464]
Humoral immune deficiency [Orphanet:47160]
Humoral immune defect (finding) [Orphanet:47160]
Deficiencies of humoral immunity (finding) [Orphanet:47160]
Humoral immune defect [Orphanet:47160]
Quality:
Cross references:
Orphanet:47160 "Agammaglobulinemia/hypogammaglobulinemia/B-cell deficiency" [Orphanet:47160]
OMIM: "Agammaglobulinemia" [OMIM:Agammaglobulinemia]
OMIM: "Hypogammaglobulinemia (1 patient)" [OMIM:Hypogammaglobulinemia (1 patient)]
UMLS:C0001768 "Agammaglobulinaemia" [HPO:0004432]
UMLS:C0001768 "Agammaglobulinemia" [Orphanet:47160]
UMLS:C0522274 "Humoral immune defect" [Orphanet:47160]
Is a (Direct Parents):
HPO         Decreased antibody level in blood
MedDRA Primary immunodeficiency syndromes
Orphanet Decreased antibody level in blood
Orphanet Recurrent bacterial infections
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Abnormality of humoral immunity(HPO:0005368)
                Abnormal immunoglobulin level(HPO:0010701)
                   Decreased antibody level in blood(HPO:0004313)
                      Agammaglobulinemia(HPO:0004432)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Abnormality of lymphocytes(HPO:0004332)
                   Abnormality of B cells(HPO:0002846)
                      Abnormality of B cell physiology(HPO:0005372)
                         Abnormal immunoglobulin level(HPO:0010701)
                            Decreased antibody level in blood(HPO:0004313)
                               Agammaglobulinemia(HPO:0004432)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Abnormality of lymphocytes(HPO:0004332)
                Abnormality of B cells(HPO:0002846)
                   Abnormality of B cell physiology(HPO:0005372)
                      Abnormal immunoglobulin level(HPO:0010701)
                         Decreased antibody level in blood(HPO:0004313)
                            Agammaglobulinemia(HPO:0004432)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Immunodeficiency syndromes(MedDRA:10021460)
       Primary immunodeficiency syndromes(MedDRA:10036700)
          Agammaglobulinemia(HPO:0004432)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE (OMIM:601495)
AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE (OMIM:613500)
AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE (OMIM:613501)
AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE (OMIM:613502)
AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT (OMIM:613506)
AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE (OMIM:612692)
AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE (OMIM:615214)
AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2 (OMIM:300310)
Autosomal agammaglobulinemia (Orphanet:33110)
Bloom syndrome (Orphanet:125)
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl (OMIM:614576)
IMMUNODEFICIENCY 15 (OMIM:615592)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
Isolated agammaglobulinemia (Orphanet:229717)
Short-limb skeletal dysplasia with severe combined immunodeficiency (Orphanet:935)
T-B+ severe combined immunodeficiency due to gamma chain deficiency (Orphanet:276)