PedAM
Pediatric Disease Annotations & Medicines
| acute pyelonephritis | ||||
| Disease ID | 1763 |
|---|---|
| Disease | acute pyelonephritis |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:18) HP:0100699 | Scarring | 7 HP:0001919 | Acute renal failure | 5 HP:0000010 | Frequent urinary tract infections | 3 HP:0100806 | Sepsis | 3 HP:0000819 | Diabetes mellitus | 2 HP:0000083 | Renal insufficiency | 1 HP:0030731 | Carcinoma | 1 HP:0001397 | Hepatic steatosis | 1 HP:0001903 | Anemia | 1 HP:0011779 | Anaplastic thyroid carcinoma | 1 HP:0001945 | Fever | 1 HP:0000121 | Nephrocalcinosis | 1 HP:0000138 | Ovarian cyst | 1 HP:0012461 | Bacteria in urine | 1 HP:0006573 | Acute fatty liver | 1 HP:0002890 | Thyroid carcinoma | 1 HP:0000076 | Vesicoureteric reflux | 1 HP:0000126 | Hydronephrosis | 1 |
| Disease ID | 1763 |
|---|---|
| Disease | acute pyelonephritis |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:5) C0004610 | bacteremia | 6 C0036690 | sepsis | 3 C1096262 | escherichia coli bacteremia | 1 C0015967 | fever | 1 C0022660 | acute renal failure | 1 |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
All Snps(Total Genotypes:2) | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
| rs3804099 | 23484049 | 7097 | TLR2 | umls:C0520575 | BeFree | Further genotype pattern frequency analysis in TLR-2 SNPs (rs3804099 and rs3804100) showed significantly reduced occurrence of the rare allele homozygote (CC+CC) in the no-VUR subgroup of APN and ALN cases. | 0.000271442 | 2013 | TLR2 | 4 | 153703504 | T | C |
| rs3804100 | 23484049 | 7097 | TLR2 | umls:C0520575 | BeFree | Further genotype pattern frequency analysis in TLR-2 SNPs (rs3804099 and rs3804100) showed significantly reduced occurrence of the rare allele homozygote (CC+CC) in the no-VUR subgroup of APN and ALN cases. | 0.000271442 | 2013 | TLR2 | 4 | 153704257 | 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.) |
Chemical(Total Drugs:0) | |
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| (Waiting for update.) | |
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.) | |