PedAM
Pediatric Disease Annotations & Medicines
| peripheral t-cell lymphoma | ||||
| Disease ID | 617 |
|---|---|
| Disease | peripheral t-cell lymphoma |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:14) HP:0002665 | Lymphoma | 3 HP:0012190 | T cell lymphoma | 2 HP:0100280 | Morbus Crohn | 1 HP:0011919 | Pleural empyema | 1 HP:0002242 | Enteropathy | 1 HP:0100008 | Schwann cell tumour | 1 HP:0009125 | Lipodystrophy | 1 HP:0011974 | Myelofibrosis | 1 HP:0001888 | Lymphocytopenia | 1 HP:0001399 | Liver failure | 1 HP:0005523 | Lymphoproliferative disorder | 1 HP:0000999 | Pyoderma | 1 HP:0002608 | Celiac disease | 1 HP:0006554 | Acute hepatic failure | 1 |
| Disease ID | 617 |
|---|---|
| Disease | peripheral t-cell lymphoma |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:4) |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
All Snps(Total Genotypes:3) | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
| rs113488022 | 24689848 | 387 | RHOA | umls:C0079774 | BeFree | They include the V600E BRAF mutation in hairy cell leukemia, the L265P MYD88 mutation in Waldenström macroglobulinemia, the G17V RHOA mutation in angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma, not otherwise specified, and the Y640F//D661Y/V/H/I//N647I STAT3 mutations in T-cell large granular lymphocytic leukemia. | 0.120814326 | 2014 | BRAF | 7 | 140753336 | A | T,G,C |
| rs371896760 | 24689848 | 387 | RHOA | umls:C0079774 | BeFree | They include the V600E BRAF mutation in hairy cell leukemia, the L265P MYD88 mutation in Waldenström macroglobulinemia, the G17V RHOA mutation in angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma, not otherwise specified, and the Y640F//D661Y/V/H/I//N647I STAT3 mutations in T-cell large granular lymphocytic leukemia. | 0.120814326 | 2014 | ACAA1;MYD88 | 3 | 38138714 | G | T |
| rs387907272 | 24689848 | 387 | RHOA | umls:C0079774 | BeFree | They include the V600E BRAF mutation in hairy cell leukemia, the L265P MYD88 mutation in Waldenström macroglobulinemia, the G17V RHOA mutation in angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma, not otherwise specified, and the Y640F//D661Y/V/H/I//N647I STAT3 mutations in T-cell large granular lymphocytic leukemia. | 0.120814326 | 2014 | MYD88 | 3 | 38141150 | T | C |
GWASdb Annotation(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
|---|---|
| (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:2) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| CUI | ChemicalName | ChemicalID | CasRN | DiseaseName | DiseaseID | DirectEvidence | PubMedIDs | ||
| C0079774 | belinostat | C487081 | - | lymphoma, t-cell, peripheral | MESH:D016411 | therapeutic | 23382909 | ||
| C0079774 | mitoxantrone | D008942 | 65271-80-9 | lymphoma, t-cell, peripheral | MESH:D016411 | therapeutic | 17052256 | ||
FDA approved drug and dosage information(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |