thrombocytopenia |
Disease ID | 553 |
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Disease | thrombocytopenia |
Manually Symptom | UMLS | Name(Total Manually Symptoms:82) C2707258 | infections C2697310 | sarcoidosis C2364133 | infection C2364050 | hypothermia C2186532 | liver disease C1962966 | retinopathy C1962958 | hematoma C1660219 | analgesia C1623038 | cirrhosis C1521999 | acute myocardial infarction C1509147 | histiocytoma C1508749 | capillary fragility C1443043 | myeloproliferative syndromes C1387528 | acute hemolytic anemia C1384590 | hemangiomatosis C1333817 | giant hemangioma C1275974 | splenic hamartoma C1275974 | hamartoma of spleen C1268935 | microangiopathic hemolytic anemia C1142517 | lupus anticoagulant C1027109 | scleroderma C0948824 | hemorrhagic anemia C0948089 | acute coronary syndrome C0917798 | cerebral ischemia C0878643 | epiphenomenon C0796110 | w syndrome C0796095 | c syndrome C0728731 | prematurity C0685201 | splenic hemangioma C0600502 | hemostatic disorders C0398686 | primary immunodeficiency C0346424 | splenic angiosarcoma C0338575 | sagittal sinus thrombosis C0334121 | inflammatory myofibroblastic tumor C0282607 | vascular tumors C0272412 | splenic abscess C0267373 | intestinal bleeding C0265053 | lower extremity thrombophlebitis C0221025 | kasabach-merritt syndrome C0221021 | microangiopathic haemolytic anaemia C0206255 | malaria C0152915 | disseminated tuberculosis C0151945 | cerebral vein thrombosis C0085669 | acute leukemia C0085278 | antiphospholipid syndrome C0042974 | von willebrand's disease C0040156 | thyrotoxicosis C0040053 | thrombosis C0035021 | relapsing fever C0034150 | purpuras C0034150 | purpura C0032285 | pneumonia C0032001 | pituitary apoplexy C0031256 | petechiae C0029927 | ovarian cyst C0029166 | oral manifestations C0027051 | myocardial infarction C0026848 | myopathy C0026691 | kawasaki disease C0023794 | lipidosis C0023418 | leukemia C0021051 | immunodeficiency disorder C0021051 | immunodeficiency C0020532 | hypersplenism C0019693 | hiv infection C0019618 | histiocytosis C0019189 | chronic hepatitis C0019101 | hemorrhagic fever with renal syndrome C0019087 | hemorrhagic diathesis C0019087 | haemorrhagic diathesis C0019080 | hemorrhage C0018916 | hemangiomas C0018916 | hemangioma C0017181 | gastrointestinal hemorrhage C0010823 | cmv infection C0006309 | brucellosis C0005956 | bone marrow disease C0005818 | platelet disorders C0005818 | blood platelet disorders C0005779 | coagulopathy C0002879 | acquired hemolytic anemia C0002878 | hemolytic anemia |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:40) C0040053 | thrombosis | 41 C0009450 | infection | 31 C0002878 | hemolytic anemia | 27 C0019080 | hemorrhage | 22 C0023895 | liver disease | 22 C0019189 | chronic hepatitis | 20 C0023890 | cirrhosis | 16 C0024530 | malaria | 15 C0796095 | c syndrome | 15 C0023418 | leukemia | 12 C0020532 | hypersplenism | 12 C0005779 | coagulopathy | 11 C0221021 | microangiopathic hemolytic anemia | 8 C0034150 | purpura | 8 C0021311 | infections | 7 C0267373 | intestinal bleeding | 6 C0948089 | acute coronary syndrome | 5 C0020672 | hypothermia | 4 C0085278 | antiphospholipid syndrome | 3 C0021051 | immunodeficiency | 3 C0398686 | primary immunodeficiency | 3 C0032285 | pneumonia | 3 C0085669 | acute leukemia | 3 C0006309 | brucellosis | 2 C0027051 | myocardial infarction | 2 C0221021 | microangiopathic haemolytic anaemia | 2 C0018916 | hemangiomas | 2 C0019087 | hemorrhagic diathesis | 2 C0035309 | retinopathy | 1 C0728731 | prematurity | 1 C0085240 | lupus anticoagulant | 1 C0346424 | splenic angiosarcoma | 1 C0221025 | kasabach-merritt syndrome | 1 C0031256 | petechiae | 1 C0032001 | pituitary apoplexy | 1 C0019101 | hemorrhagic fever with renal syndrome | 1 C0018944 | hematoma | 1 C0010823 | cmv infection | 1 C0021051 | immunodeficiency disorder | 1 C0036202 | sarcoidosis | 1 |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:2) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs786205154 | NA | 2120 | ETV6 | umls:C0040034 | CLINVAR | NA | 0.24 | NA | ETV6 | 12 | 11885921 | AACAG | - |
rs786205155 | NA | 2120 | ETV6 | umls:C0040034 | CLINVAR | NA | 0.24 | NA | ETV6 | 12 | 11884481 | T | C |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Disease ID | 553 |
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Disease | thrombocytopenia |
Case | (Waiting for update.) |