leukemia, t-cell, chronic |
Disease ID | 1737 |
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Disease | leukemia, t-cell, chronic |
Definition | A slow-growing type of leukemia (blood cancer) in which too many lymphocytes are found in the bone marrow and/or blood. The T-cell is specified as the defective cell line. |
Synonym | chronic t-cell leukemia chronic t-cell lymphocytic leukemia cll, t-cell leukemia, lymphocytic, chronic, t cell leukemia, lymphocytic, chronic, t-cell leukemia, prolymphocytic, t-cell leukemia, prolymphocytic, t-cell [disease/finding] leukemia, t cell, chronic lymphocytic leukemia, t cell, chronic lymphocytic leukemia, t-cell, chronic t cell chronic lymphocytic leukemia t cell cll t-cell chronic lymphocytic leukaemia t-cell chronic lymphocytic leukemia t-cell chronic lymphocytic leukemia (disorder) t-cell cll t-cell leukemia, chronic t-cell prolymphocytic leukemia t-lymphocytic leukemia, chronic tcll - t-cell chronic lymphocytic leukaemia tcll - t-cell chronic lymphocytic leukemia |
Orphanet | |
UMLS | C0023494 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:6) C0024299 | lymphoma | 2 C0019829 | hodgkin's lymphoma | 1 C0017601 | glaucoma | 1 C0079744 | diffuse large b-cell lymphoma | 1 C0042384 | vasculitis | 1 C0079731 | b-cell lymphoma | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | (Waiting for update.) |
Locus | (Waiting for update.) |
Disease ID | 1737 |
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Disease | leukemia, t-cell, chronic |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:5) HP:0002665 | Lymphoma | 2 HP:0000501 | Glaucoma | 1 HP:0012189 | Hodgkin disease | 1 HP:0012191 | B-cell lymphoma | 1 HP:0002633 | Vasculitis | 1 |
Disease ID | 1737 |
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Disease | leukemia, t-cell, chronic |
Manually Symptom | (Waiting for update.) |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
All Snps(Total Genotypes:3) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs121434217 | NA | 472 | ATM | umls:C2363142 | CLINVAR | NA | 0.125700279 | NA | ATM | 11 | 108299752 | G | C |
rs121434223 | NA | 472 | ATM | umls:C2363142 | CLINVAR | NA | 0.125700279 | NA | ATM | 11 | 108301779 | C | G |
rs28904921 | NA | 472 | ATM | umls:C2363142 | CLINVAR | NA | 0.125700279 | NA | ATM | 11 | 108329202 | T | 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 | ||
C0023494 | bortezomib | D000069286 | - | leukemia, prolymphocytic, t-cell | MESH:D015461 | therapeutic | 17990182 |
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.) |