interdigitating dendritic cell sarcoma |
Disease ID | 1633 |
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Disease | interdigitating dendritic cell sarcoma |
Definition | rare type of nonHodgkin's lymphoma of intermediate to high malignancy, characterized by the presence of large tumor cells that resemble histiocytes morphologically but are considered to be of lymphoid origin. |
Synonym | [m] large cell lymphoma [m] large cell lymphoma (morphologic abnormality) [m]reticulosarcoma nos cell large lymphomas cell reticulum sarcomas cells reticulum sarcoma histiocytic lymphoma interdigitating cell sarcoma interdigitating dendritic cell sarcoma (disorder) large cell lymphoma lymphoma large cell malignant lymphoma reticulum cell type reticulosarcoma reticulosarcoma (clinical) [obsolete] reticulosarcoma (clinical) [obsolete] (disorder) reticulosarcoma (disorder) reticulosarcoma (morphologic abnormality) reticulosarcoma -retired- reticulosarcoma morphology reticulosarcoma morphology (disorder) reticulosarcoma morphology (morphologic abnormality) reticulosarcoma nos reticulosarcoma nos (disorder) reticulosarcoma of unspecified site reticulosarcoma of unspecified site (disorder) reticulosarcoma, diffuse reticulosarcoma, nos reticulosarcomas reticulum cell sarcoma reticulum cell sarcoma morphol reticulum cell sarcoma morphology reticulum cell sarcoma nos reticulum cell sarcoma, diffuse reticulum cell sarcoma, nos reticulum-cell sarcoma reticulum-cell sarcomas sarcoma, reticulum cell sarcoma, reticulum-cell sarcomas, reticulum-cell |
Orphanet | |
OMIM | |
DOID | |
UMLS | C0024302 |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:30) C0024299 | lymphoma | 3 C0026986 | myelodysplastic syndrome | 2 C0011603 | dermatitis | 2 C0023434 | chronic lymphocytic leukemia | 2 C0024291 | hemophagocytic lymphohistiocytosis | 2 C0023448 | lymphocytic leukemia | 2 C0032285 | pneumonia | 1 C0085113 | neurofibromatosis | 1 C0026986 | myelodysplastic syndromes | 1 C0598894 | monocytic leukemia | 1 C0019829 | hodgkin lymphoma | 1 C0079731 | b-cell lymphoma | 1 C0027121 | myositis | 1 C0024291 | hemophagocytic syndrome | 1 C0013990 | emphysema | 1 C0030807 | pemphigus | 1 C0343084 | capillary leak syndrome | 1 C0079419 | li-fraumeni syndrome | 1 C0553662 | juvenile idiopathic arthritis | 1 C0030805 | pemphigoid | 1 C0553662 | juvenile arthritis | 1 C0011615 | atopic dermatitis | 1 C0242647 | mucosa-associated lymphoid tissue | 1 C0079731 | b-cell lymphomas | 1 C0003873 | rheumatoid arthritis | 1 C0011608 | dermatitis herpetiformis | 1 C0041296 | tuberculosis | 1 C0002878 | hemolytic anemia | 1 C0030805 | bullous pemphigoid | 1 C0002880 | autoimmune hemolytic anemia | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:126) 8227 | AKAP17A | 1.526 | DISEASES 238 | ALK | 6.236 | DISEASES 257 | ALX3 | 2.181 | DISEASES 2909 | ARHGAP35 | 1.346 | DISEASES 196528 | ARID2 | 2.899 | DISEASES 567 | B2M | 1.834 | DISEASES 9532 | BAG2 | 1.575 | DISEASES 800 | CALD1 | 1.633 | DISEASES 896 | CCND3 | 2.004 | DISEASES 8812 | CCNK | 1.863 | DISEASES 9332 | CD163 | 3.371 | DISEASES 930 | CD19 | 1.962 | DISEASES 910 | CD1B | 2.413 | DISEASES 911 | CD1C | 1.527 | DISEASES 914 | CD2 | 2.589 | DISEASES 50489 | CD207 | 2.117 | DISEASES 951 | CD37 | 1.814 | DISEASES 916 | CD3E | 1.109 | DISEASES 917 | CD3G | 1.127 | DISEASES 959 | CD40LG | 1.827 | DISEASES 960 | CD44 | 1.692 | DISEASES 921 | CD5 | 2.711 | DISEASES 1043 | CD52 | 1.961 | DISEASES 1029 | CDKN2A | 1.097 | DISEASES 1032 | CDKN2D | 1.064 | DISEASES 1050 | CEBPA | 1.341 | DISEASES 1314 | COPA | 1.332 | DISEASES 1378 | CR1 | 3.166 | DISEASES 1378 | CR1 | 1.641 | DISEASES 1380 | CR2 | 4.582 | DISEASES 1380 | CR2 | 1.634 | DISEASES 64764 | CREB3L2 | 1.967 | DISEASES 1791 | DNTT | 1.719 | DISEASES 56940 | DUSP22 | 3.886 | DISEASES 1870 | E2F2 | 1.582 | DISEASES 27436 | EML4 | 3.009 | DISEASES 2130 | EWSR1 | 1.035 | DISEASES 2197 | FAU | 1.477 | DISEASES 2235 | FECH | 1.872 | DISEASES 2268 | FGR | 1.671 | DISEASES 6624 | FSCN1 | 4.038 | DISEASES 6624 | FSCN1 | 1.583 | DISEASES 2526 | FUT4 | 3.192 | DISEASES 2621 | GAS6 | 1.335 | DISEASES 28964 | GIT1 | 1.502 | DISEASES 2885 | GRB2 | 2.813 | DISEASES 3005 | H1F0 | 1.129 | DISEASES 51696 | HECA | 2.146 | DISEASES 3200 | HOXA3 | 1.761 | DISEASES 3347 | HTN3 | 1.601 | DISEASES 219844 | HYLS1 | 2.246 | DISEASES 3559 | IL2RA | 1.596 | DISEASES 3563 | IL3RA | 2.566 | DISEASES 3662 | IRF4 | 2.372 | DISEASES 3676 | ITGA4 | 1.62 | DISEASES 3683 | ITGAL | 1.3 | DISEASES 3702 | ITK | 1.403 | DISEASES 23210 | JMJD6 | 2.143 | DISEASES 3725 | JUN | 1.157 | DISEASES 3735 | KARS | 1.129 | DISEASES 3812 | KIR3DL2 | 1.299 | DISEASES 3932 | LCK | 2.432 | DISEASES 51213 | LUZP4 | 1.866 | DISEASES 4065 | LY75 | 2.449 | DISEASES 4170 | MCL1 | 1.377 | DISEASES 4311 | MME | 2.253 | DISEASES 9242 | MSC | 1.45 | DISEASES 4478 | MSN | 1.157 | DISEASES 4601 | MXI1 | 1.186 | DISEASES 4609 | MYC | 3.339 | DISEASES 4772 | NFATC1 | 1.03 | DISEASES 4773 | NFATC2 | 2.135 | DISEASES 64332 | NFKBIZ | 1.267 | DISEASES 7025 | NR2F1 | 1.025 | DISEASES 50814 | NSDHL | 1.967 | DISEASES 5079 | PAX5 | 2.184 | DISEASES 5079 | PAX5 | 1.347 | DISEASES 5111 | PCNA | 2.061 | DISEASES 9260 | PDLIM7 | 2.47 | DISEASES 5450 | POU2AF1 | 1.045 | DISEASES 639 | PRDM1 | 1.827 | DISEASES 5583 | PRKCH | 1.143 | DISEASES 5764 | PTN | 1.826 | DISEASES 5787 | PTPRB | 2.254 | DISEASES 5788 | PTPRC | 4.02 | DISEASES 5788 | PTPRC | 3.735 | DISEASES 5796 | PTPRK | 1.538 | DISEASES 5803 | PTPRZ1 | 1.999 | DISEASES 399 | RHOH | 1.366 | DISEASES 49855 | SCAPER | 2.426 | DISEASES 10507 | SEMA4D | 1.004 | DISEASES 5265 | SERPINA1 | 2.776 | DISEASES 12 | SERPINA3 | 2.499 | DISEASES 5272 | SERPINB9 | 1.067 | DISEASES 6421 | SFPQ | 1.424 | DISEASES 6464 | SHC1 | 1.69 | DISEASES 347734 | SLC35B2 | 2.186 | DISEASES 347734 | SLC35B2 | 2.101 | DISEASES 6520 | SLC3A2 | 1.456 | DISEASES 23583 | SMUG1 | 1.245 | DISEASES 6622 | SNCA | 2.657 | DISEASES 6663 | SOX10 | 2.01 | DISEASES 6693 | SPN | 3.445 | DISEASES 6714 | SRC | 1.723 | DISEASES 6759 | SSX4 | 1.3 | DISEASES 548313 | SSX4B | 1.306 | DISEASES 90627 | STARD13 | 1.013 | DISEASES 6847 | SYCP1 | 1.954 | DISEASES 7037 | TFRC | 1.704 | DISEASES 7072 | TIA1 | 4.039 | DISEASES 3195 | TLX1 | 1.771 | DISEASES 7124 | TNF | 1.444 | DISEASES 7127 | TNFAIP2 | 1.463 | DISEASES 10188 | TNK2 | 1.263 | DISEASES 7170 | TPM3 | 3.694 | DISEASES 7185 | TRAF1 | 2.472 | DISEASES 22954 | TRIM32 | 1.104 | DISEASES 80328 | ULBP2 | 1.074 | DISEASES 79465 | ULBP3 | 1.518 | DISEASES 7410 | VAV2 | 1.27 | DISEASES 10451 | VAV3 | 1.106 | DISEASES 7499 | XG | 1.586 | DISEASES 7525 | YES1 | 1.058 | DISEASES 10773 | ZBTB6 | 2.657 | DISEASES 340152 | ZC3H12D | 1.812 | DISEASES 22834 | ZNF652 | 2.069 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1633 |
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Disease | interdigitating dendritic cell sarcoma |
Integrated Phenotype | HPO | Name(Total Integrated Phenotypes:1) HP:0100242 | Sarcoma |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:21) HP:0002665 | Lymphoma | 4 HP:0002863 | Myelodysplastic syndrome | 2 HP:0005550 | Chronic lymphatic leukemia | 2 HP:0002664 | Neoplasia | 2 HP:0002090 | Pneumonia | 1 HP:0002835 | Aspiration | 1 HP:0012189 | Hodgkin disease | 1 HP:0001067 | Neurofibromas | 1 HP:0004820 | Acute myelomonocytic leukemia | 1 HP:0005681 | Juvenile idiopathic arthritis | 1 HP:0001370 | Rheumatoid arthritis | 1 HP:0001878 | Haemolytic anaemia | 1 HP:0012191 | B-cell lymphoma | 1 HP:0001047 | Atopic dermatitis | 1 HP:0001890 | Autoimmune hemolytic anemia | 1 HP:0100614 | Muscle inflammation | 1 HP:0030731 | Carcinoma | 1 HP:0005200 | Retroperitoneal fibrosis | 1 HP:0002097 | Pulmonary emphysema | 1 HP:0001482 | Subcutaneous nodule | 1 HP:0001114 | Fatty deposits on eyelids | 1 |
Disease ID | 1633 |
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Disease | interdigitating dendritic cell sarcoma |
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.) |
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:1) | ||||
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HP ID | HP Name | MP ID | MP Name | Annotation |
HP:0100242 | Sarcoma | MP:0020329 | decreased capillary density | reduction in the number of capillaries in a given cross-sectional area of a tissue |
Disease ID | 1633 |
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Disease | interdigitating dendritic cell sarcoma |
Case | (Waiting for update.) |