strongyloidiasis |
Disease ID | 1217 |
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Disease | strongyloidiasis |
Definition | Infection with nematodes of the genus STRONGYLOIDES. The presence of larvae may produce pneumonitis and the presence of adult worms in the intestine could lead to moderate to severe diarrhea. |
Synonym | [x]strongyloidiasis, unspecified [x]strongyloidiasis, unspecified (disorder) infection by strongyloides infection by strongyloides (disorder) infection by strongyloides, nos infection caused by strongyloides infection caused by strongyloides (disorder) strongylodiasis strongyloides infection strongyloidiases strongyloidiasis [disease/finding] strongyloidosis |
Orphanet | |
DOID | |
UMLS | C0038463 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:17) C0025289 | meningitis | 3 C0085437 | bacterial meningitis | 2 C0235618 | proliferative glomerulonephritis | 2 C0017658 | glomerulonephritis | 2 C0017662 | membranoproliferative glomerulonephritis | 2 C1522378 | large granular lymphocytosis | 1 C0024141 | systemic lupus erythematosus | 1 C0002871 | anemia | 1 C0017536 | giardiasis | 1 C0178238 | intestinal infections | 1 C0001973 | alcoholism | 1 C0042769 | virus infection | 1 C0035435 | rheumatic diseases | 1 C0035435 | rheumatic disease | 1 C0409974 | lupus erythematosus | 1 C0036323 | schistosomiasis | 1 C0178238 | intestinal infection | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:30) 279 | AMY2A | 2.164 | DISEASES 408 | ARRB1 | 2.116 | DISEASES 833 | CARS | 1.739 | DISEASES 959 | CD40LG | 2.251 | DISEASES 80781 | COL18A1 | 1.176 | DISEASES 255324 | EPGN | 2.189 | DISEASES 2213 | FCGR2B | 1.626 | DISEASES 2235 | FECH | 1.993 | DISEASES 2623 | GATA1 | 1.332 | DISEASES 3329 | HSPD1 | 1.227 | DISEASES 3418 | IDH2 | 1.351 | DISEASES 29949 | IL19 | 2.308 | DISEASES 90865 | IL33 | 1.282 | DISEASES 3712 | IVD | 3.606 | DISEASES 84946 | LTV1 | 3.782 | DISEASES 4512 | MT-CO1 | 2.683 | DISEASES 4843 | NOS2 | 1.139 | DISEASES 4521 | NUDT1 | 2.281 | DISEASES 4942 | OAT | 1.592 | DISEASES 7932 | OR2H2 | 4.097 | DISEASES 11201 | POLI | 2.041 | DISEASES 56342 | PPAN | 2.692 | DISEASES 56980 | PRDM10 | 1.576 | DISEASES 404552 | SCGB1D4 | 2.184 | DISEASES 6518 | SLC2A5 | 2.383 | DISEASES 503542 | SPRN | 2.616 | DISEASES 246744 | STH | 1.955 | DISEASES 9623 | TCL1B | 3.323 | DISEASES 7110 | TMF1 | 2.676 | DISEASES 127262 | TPRG1L | 2.953 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1217 |
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Disease | strongyloidiasis |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:12) HP:0001880 | Eosinophilia | 4 HP:0000793 | Membranoproliferative glomerulonephritis | 2 HP:0000099 | Glomerular nephritis | 2 HP:0001287 | Meningitis | 2 HP:0001945 | Fever | 1 HP:0002716 | Lymph node hyperplasia | 1 HP:0002725 | Systemic lupus erythematosus | 1 HP:0002584 | Intestinal hemorrhage | 1 HP:0001903 | Anemia | 1 HP:0100806 | Sepsis | 1 HP:0003146 | Decreased circulating cholesterol level | 1 HP:0002239 | Gastrointestinal hemorrhage | 1 |
Disease ID | 1217 |
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Disease | strongyloidiasis |
Manually Symptom | UMLS | Name(Total Manually Symptoms:28) C2240374 | eosinophilia C1963165 | malabsorption C1963084 | colitis C1839611 | n syndrome C1704321 | minimal change nephrotic syndrome C1522057 | duodenitis C1384353 | parasitic infestation C1257845 | pseudomembranous enteritis C1090821 | sepsis C0853793 | enterococcal meningitis C0277792 | pathognomonic sign C0267375 | chronic colitis C0264490 | acute respiratory failure C0263338 | chronic urticaria C0239182 | watery diarrhea C0033680 | protein-losing enteropathy C0030446 | paralytic ileus C0027726 | nephrotic syndrome C0024291 | hemophagocytic syndrome C0023501 | leukemoid reaction C0023048 | larva migrans C0021843 | intestinal obstruction C0021831 | enteropathy C0021141 | syndrome of inappropriate secretion of antidiuretic hormone C0020097 | htlv-i infection C0015230 | rash C0011991 | diarrhoea C0004623 | bacterial infections |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:3) C0014457 | eosinophilia | 4 C1839611 | n syndrome | 2 C0027721 | minimal change nephrotic syndrome | 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 | 1217 |
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Disease | strongyloidiasis |
Case | (Waiting for update.) |