amebiasis |
Disease ID | 618 |
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Disease | amebiasis |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:5) HP:0002013 | Emesis | 1 HP:0000126 | Hydronephrosis | 1 HP:0002583 | Colitis | 1 HP:0100523 | Hepatic abscess | 1 HP:0002721 | Immunodeficiency | 1 |
Disease ID | 618 |
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Disease | amebiasis |
Manually Symptom | UMLS | Name(Total Manually Symptoms:15) C1510428 | cerebral abscesses C0701815 | hyperchromic anemia C0267166 | gastroduodenitis C0221014 | secondary amyloidosis C0151594 | bloody diarrhea C0042850 | vitamin b complex deficiency C0038463 | strongyloidiasis C0037285 | skin manifestations C0037074 | sigmoiditis C0031154 | peritonitis C0019204 | hepatic carcinoma C0019158 | hepatitis C0008526 | choroiditis C0007137 | squamous cell carcinoma C0000727 | acute abdomen |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
All Snps(Total Genotypes:1) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs1137101 | 25516614 | 3953 | LEPR | umls:C0002438 | BeFree | Humans with the Q223R leptin receptor mutation have increased susceptibility to amebiasis, but the mechanism has been unclear. | 0.000542884 | 2015 | LEPR | 1 | 65592830 | A | G |
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.) |
Chemical(Total Drugs:1) | |||||||||
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CUI | ChemicalName | ChemicalID | CasRN | DiseaseName | DiseaseID | DirectEvidence | PubMedIDs | ||
C0002438 | tinidazole | D014011 | 19387-91-8 | amebiasis | MESH:D000562 | therapeutic | 7123 |
FDA approved drug and dosage information(Total Drugs:0) | |
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(Waiting for update.) |
FDA labeling changes(Total Drugs:0) | |
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(Waiting for update.) |