Agammaglobulinemia
Symptom Information:
Symptom ID: | HPO:0004432 | |||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) 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) MedDRA: Immune system disorders(MedDRA:10021428) Immunodeficiency syndromes(MedDRA:10021460) Primary immunodeficiency syndromes(MedDRA:10036700) Agammaglobulinemia(HPO:0004432) |
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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) |