Autoimmune thrombocytopenia
Symptom Information:
Symptom ID: | HPO:0001973 | |||||||||||
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 thrombocytes(HPO:0001872) Abnormal platelet count(HPO:0011873) Thrombocytopenia(HPO:0001873) Autoimmune thrombocytopenia(HPO:0001973) Abnormality of the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Autoimmunity(HPO:0002960) Autoimmune thrombocytopenia(HPO:0001973) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of thrombocytes(HPO:0001872) Thrombocytopenia(HPO:0001873) Autoimmune thrombocytopenia(HPO:0001973) |
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Database Frequency: | 18 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
ANTIPHOSPHOLIPID SYNDROME, FAMILIAL | (OMIM:107320) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME | (OMIM:601859) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA | (OMIM:603909) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III | (OMIM:615559) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V | (OMIM:616100) |
Alström syndrome | (Orphanet:64) |
Autoimmune lymphoproliferative syndrome | (Orphanet:3261) |
CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION | (OMIM:601389) |
Hyper-IgM syndrome type 4 | (Orphanet:101091) |
IMMUNODEFICIENCY, COMMON VARIABLE, 6 | (OMIM:613496) |
KABUKI SYNDROME 1 | (OMIM:147920) |
Kabuki syndrome | (Orphanet:2322) |
Krabbe disease | (Orphanet:487) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER | (OMIM:614470) |
SPASTIC PARAPLEGIA AND EVANS SYNDROME | (OMIM:601608) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |