IgA deficiency
Symptom Information:
Symptom ID: | HPO:0002720 | |||||||||||
Synonyms: |
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Quality: | ||||||||||||
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) IgA deficiency(HPO:0002720) Abnormality of the immune system(HPO:0002715) 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) IgA deficiency(HPO:0002720) 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) IgA deficiency(HPO:0002720) MedDRA: |
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Database Frequency: | 33 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
ATAXIA-TELANGIECTASIA | (OMIM:208900) |
ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLYDEATH | (OMIM:208910) |
Ataxia-telangiectasia | (Orphanet:100) |
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation | (Orphanet:324530) |
Bloom syndrome | (Orphanet:125) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME | (OMIM:215250) |
Common variable immunodeficiency | (Orphanet:1572) |
Dubowitz syndrome | (Orphanet:235) |
GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF | (OMIM:137050) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN | (OMIM:235500) |
Hyper-IgM syndrome type 2 | (Orphanet:101089) |
Hyper-IgM syndrome type 3 | (Orphanet:101090) |
Hyper-IgM syndrome type 5 | (Orphanet:101092) |
IMMUNE DEFICIENCY, FAMILIAL VARIABLE | (OMIM:146830) |
IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA | (OMIM:300584) |
IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
IMMUNODEFICIENCY, COMMON VARIABLE, 7 | (OMIM:614699) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
IMMUNOGLOBULIN A DEFICIENCY 1 | (OMIM:137100) |
IMMUNOGLOBULIN A DEFICIENCY 2 | (OMIM:609529) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Lichstenstein syndrome | (Orphanet:2390) |
Lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis | (Orphanet:137631) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
Monosomy 18q | (Orphanet:1600) |
PMM2-CDG | (Orphanet:79318) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Transcobalamin deficiency | (Orphanet:859) |
X-linked hyper-IgM syndrome | (Orphanet:101088) |