malignant histiocytosis |
Disease ID | 1882 |
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Disease | malignant histiocytosis |
Definition | A rare, usually progressive disorder comprising an invasive proliferation of neoplastic HISTIOCYTES. Many previous cases are now thought to represent ANAPLASTIC LARGE-CELL LYMPHOMA. |
Synonym | [m]malignant histiocytosis [m]malignant histiocytosis (morphologic abnormality) [m]malignant reticulosis angiocentric lymphoma angiocentric t-cell lymphoma histiocytic medullary reticulosis histiocytoses, malignant histiocytosis malignant histiocytosis, malignant lymphoma nasal t-cell malignant histiocytoses malignant histiocytosis (clinical) malignant histiocytosis (disorder) malignant histiocytosis (morphologic abnormality) malignant histiocytosis -retired- malignant histiocytosis nos malignant histiocytosis nos (disorder) malignant midline reticulosis malignant reticuloendotheliosis malignant reticulosis malignant reticulosis, nos nasal t-cell lymphoma polymorphic reticulosis reticulosis, aleukemic reticulosis, malignant reticulosis, malignant midline reticulosis, polymorphoric stewart's granuloma |
DOID | |
UMLS | C0019623 |
SNOMED-CT | |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:60) 4680 | CEACAM6 | DISEASES 6948 | TCN2 | DISEASES 54 | ACP5 | DISEASES 973 | CD79A | DISEASES 4254 | KITLG | DISEASES 968 | CD68 | DISEASES 4069 | LYZ | DISEASES 9368 | SLC9A3R1 | DISEASES 3552 | IL1A | DISEASES 943 | TNFRSF8 | DISEASES 3189 | HNRNPH3 | DISEASES 51411 | BIN2 | DISEASES 3687 | ITGAX | DISEASES 63976 | PRDM16 | DISEASES 134864 | TAAR1 | DISEASES 7070 | THY1 | DISEASES 7345 | UCHL1 | DISEASES 1436 | CSF1R | DISEASES 6271 | S100A1 | DISEASES 9965 | FGF19 | DISEASES 2215 | FCGR3B | DISEASES 4869 | NPM1 | DISEASES 10206 | TRIM13 | DISEASES 5267 | SERPINA4 | DISEASES 290 | ANPEP | DISEASES 27087 | B3GAT1 | DISEASES 10855 | HPSE | DISEASES 23592 | LEMD3 | DISEASES 924 | CD7 | DISEASES 4684 | NCAM1 | DISEASES 1435 | CSF1 | DISEASES 5155 | PDGFB | DISEASES 4602 | MYB | DISEASES 6614 | SIGLEC1 | DISEASES 921 | CD5 | DISEASES 5265 | SERPINA1 | DISEASES 2526 | FUT4 | DISEASES 7037 | TFRC | DISEASES 6693 | SPN | DISEASES 9361 | LONP1 | DISEASES 1378 | CR1 | DISEASES 1380 | CR2 | DISEASES 5788 | PTPRC | DISEASES 2214 | FCGR3A | DISEASES 6280 | S100A9 | DISEASES 3713 | IVL | DISEASES 4942 | OAT | DISEASES 914 | CD2 | DISEASES 4893 | NRAS | DISEASES 5292 | PIM1 | DISEASES 2268 | FGR | DISEASES 4300 | MLLT3 | DISEASES 414 | ARSD | DISEASES 12 | SERPINA3 | DISEASES 7913 | DEK | DISEASES 50489 | CD207 | DISEASES 7124 | TNF | DISEASES 7072 | TIA1 | DISEASES 7812 | CSDE1 | DISEASES 3347 | HTN3 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1882 |
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Disease | malignant histiocytosis |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | (Waiting for update.) |
Disease ID | 1882 |
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Disease | malignant histiocytosis |
Manually Symptom | UMLS | Name(Total Manually Symptoms:19) C1145670 | respiratory failure C1096441 | trichosporon beigelii infection C0752303 | urological manifestations C0751435 | hyperphenylalaninemia C0748159 | pulmonary involvement C0456909 | blindness C0235896 | pulmonary infiltrate C0235884 | gastric perforation C0205851 | germ cell tumour C0085655 | polymyositis C0035243 | respiratory infection C0035222 | adult respiratory distress syndrome C0032587 | polyradiculoneuropathy C0032285 | pneumonia C0029166 | oral manifestations C0023443 | hairy cell leukemia C0020532 | hypersplenism C0019214 | hepatosplenomegaly C0001125 | lactic acidosis |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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All Snps(Total Genotypes:0) | |
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GWASdb Annotation(Total Genotypes:0) | |
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GWASdb Snp Trait(Total Genotypes:0) | |
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Mapped by lexical matching(Total Items:0) |
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Mapped by homologous gene(Total Items:0) |
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Chemical(Total Drugs:0) | |
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FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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