aspergillosis |
Disease ID | 928 |
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Disease | aspergillosis |
Manually Symptom | UMLS | Name(Total Manually Symptoms:26) C2707258 | infections C2364133 | infection C1963154 | renal failure C1739376 | orbital apex syndrome C1546533 | abscess C1510428 | cerebral abscess C1298681 | oxalosis C0748159 | pulmonary involvement C0333040 | fungus ball C0302148 | thrombus C0265149 | purulent pericarditis C0264265 | nasal necrosis C0259737 | adiaspiromycosis C0241950 | bowel infarction C0238790 | bone destruction C0238036 | bronchocentric granulomatosis C0149711 | hilar adenopathy C0030486 | paraplegia C0029132 | optic neuropathy C0029089 | ophthalmoplegia C0028992 | omphalitis C0025289 | meningitis C0024894 | mastitis C0019655 | histoplasmosis C0019079 | haemoptysis C0014556 | psychomotor seizure |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:5) C0009450 | infection | 13 C0021311 | infections | 3 C0333040 | fungus ball | 2 C1739376 | orbital apex syndrome | 1 C0748159 | pulmonary involvement | 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:0) | |
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(Waiting for update.) |
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 | 928 |
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Disease | aspergillosis |
Case | (Waiting for update.) |