Decreased antibody level in blood
Symptom Information:
Symptom ID: | HPO:0004313 | ||||||||||||||||||||||||||||||
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) 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) 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) MedDRA: Immune system disorders(MedDRA:10021428) Immunodeficiency syndromes(MedDRA:10021460) Primary immunodeficiency syndromes(MedDRA:10036700) Decreased antibody level in blood(HPO:0004313) |
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Database Frequency: | 47 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V | (OMIM:616100) |
Alpha-mannosidosis | (Orphanet:61) |
Bloom syndrome | (Orphanet:125) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
Combined immunodeficiency with skin granulomas | (Orphanet:157949) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 5 | (OMIM:615190) |
Dubowitz syndrome | (Orphanet:235) |
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY | (OMIM:600351) |
GCS1-CDG | (Orphanet:79330) |
GRANULOCYTOPENIA WITH IMMUNOGLOBULIN ABNORMALITY | (OMIM:233600) |
Hepatic veno-occlusive disease - immunodeficiency | (Orphanet:79124) |
ICF syndrome | (Orphanet:2268) |
IMMUNODEFICIENCY 14 | (OMIM:615513) |
IMMUNODEFICIENCY 36 | (OMIM:616005) |
IMMUNODEFICIENCY 37 | (OMIM:616098) |
IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
IMMUNODEFICIENCY, COMMON VARIABLE, 10 | (OMIM:615577) |
IMMUNODEFICIENCY, COMMON VARIABLE, 11 | (OMIM:615767) |
IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
IMMUNODEFICIENCY, COMMON VARIABLE, 3 | (OMIM:613493) |
IMMUNODEFICIENCY, COMMON VARIABLE, 4 | (OMIM:613494) |
IMMUNODEFICIENCY, COMMON VARIABLE, 5 | (OMIM:613495) |
IMMUNODEFICIENCY, COMMON VARIABLE, 6 | (OMIM:613496) |
IMMUNODEFICIENCY, COMMON VARIABLE, 7 | (OMIM:614699) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES | (OMIM:242870) |
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2 | (OMIM:614069) |
IMMUNOERYTHROMYELOID HYPOPLASIA | (OMIM:242880) |
Intestinal lymphangiectasia | (Orphanet:36204) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
LYMPHOPROLIFERATIVE SYNDROME 1 | (OMIM:613011) |
LYMPHOPROLIFERATIVE SYNDROME 2 | (OMIM:615122) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
Osteopetrosis - hypogammaglobulinemia | (Orphanet:178389) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA | (OMIM:267900) |
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS,AND DEVELOPMENTAL DELAY | (OMIM:616084) |
SPONASTRIME dysplasia | (Orphanet:93357) |
Severe combined immunodeficiency due to CARD11 deficiency | (Orphanet:357237) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE | (OMIM:601675) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Vici syndrome | (Orphanet:1493) |
WHIM syndrome | (Orphanet:51636) |
Wolfram syndrome 2 | (OMIM:604928) |
X-linked lymphoproliferative disease | (Orphanet:2442) |