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encyclopedia of Rare Disease Annotation for Precision Medicine

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	gliosarcoma

Disease ID	1509
Disease	gliosarcoma
Definition	Rare mixed tumors of the brain and rarely the spinal cord which contain malignant neuroectodermal (glial) and mesenchymal components, including spindle-shaped fibrosarcoma cells. These tumors are highly aggressive and present primarily in adults as rapidly expanding mass lesions. They may arise in tissue that has been previously irradiated. (From Br J Neurosurg 1995 Apr;9(2):171-8)
Synonym	[m]gliosarcoma glioblastoma with a sarcomatous component glioblastoma with sarcomatous component glioblastoma with sarcomatous component (disorder) glioma, sarcomatous gliomas, sarcomatous gliosarcoma (morphologic abnormality) gliosarcoma [disease/finding] gliosarcomas sarcomatous glioma sarcomatous gliomas
Orphanet	ORPHANET:251576
DOID	DOID:3071
UMLS	C0206726
MeSH	D018316
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:5) C0206655 \| alveolar rhabdomyosarcoma \| 1 C1261473 \| sarcomas \| 1 C0035412 \| rhabdomyosarcoma \| 1 C0028945 \| oligodendroglioma \| 1 C0206093 \| primitive neuroectodermal tumor \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:15) 2260 \| FGFR1 \| ORPHANET 2261 \| FGFR3 \| ORPHANET 3417 \| IDH1 \| ORPHANET 7422 \| VEGFA \| CTD_human 1956 \| EGFR \| ORPHANET 7157 \| TP53 \| ORPHANET 5468 \| PPARG \| ORPHANET 4255 \| MGMT \| ORPHANET 5447 \| POR \| CTD_human 1555 \| CYP2B6 \| CTD_human 10460 \| TACC3 \| ORPHANET 8216 \| LZTR1 \| ORPHANET 4792 \| NFKBIA \| ORPHANET 1562 \| CYP2C18 \| CTD_human 6867 \| TACC1 \| ORPHANET
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:59) 2334 \| AFF2 \| 1.108 \| DISEASES 309 \| ANXA6 \| 1.6 \| DISEASES 8905 \| AP1S2 \| 3.483 \| DISEASES 23545 \| ATP6V0A2 \| 1.415 \| DISEASES 63827 \| BCAN \| 1.936 \| DISEASES 8945 \| BTRC \| 1.192 \| DISEASES 779 \| CACNA1S \| 1.371 \| DISEASES 887 \| CCKBR \| 1.012 \| DISEASES 896 \| CCND3 \| 1.541 \| DISEASES 1029 \| CDKN2A \| 2.094 \| DISEASES 80781 \| COL18A1 \| 2.484 \| DISEASES 1351 \| COX8A \| 1.623 \| DISEASES 1503 \| CTPS1 \| 1.924 \| DISEASES 56474 \| CTPS2 \| 3.025 \| DISEASES 1555 \| CYP2B6 \| 2.848 \| DISEASES 1576 \| CYP3A4 \| 1.848 \| DISEASES 1580 \| CYP4B1 \| 2.175 \| DISEASES 168400 \| DDX53 \| 1.198 \| DISEASES 1870 \| E2F2 \| 1.205 \| DISEASES 1896 \| EDA \| 2.234 \| DISEASES 80153 \| EDC3 \| 3.03 \| DISEASES 10480 \| EIF3M \| 2.931 \| DISEASES 2108 \| ETFA \| 1.646 \| DISEASES 2157 \| F8 \| 1.968 \| DISEASES 2187 \| FANCB \| 1.656 \| DISEASES 2550 \| GABBR1 \| 1.767 \| DISEASES 8811 \| GALR2 \| 1.703 \| DISEASES 85476 \| GFM1 \| 1.62 \| DISEASES 3091 \| HIF1A \| 1.215 \| DISEASES 3161 \| HMMR \| 1.101 \| DISEASES 3320 \| HSP90AA1 \| 1.252 \| DISEASES 3326 \| HSP90AB1 \| 2.907 \| DISEASES 3418 \| IDH2 \| 2.339 \| DISEASES 2537 \| IFI6 \| 2.172 \| DISEASES 8519 \| IFITM1 \| 1.527 \| DISEASES 9636 \| ISG15 \| 1.081 \| DISEASES 10186 \| LHFP \| 3.002 \| DISEASES 440900 \| LINC01191 \| 1.215 \| DISEASES 4193 \| MDM2 \| 1.82 \| DISEASES 4600 \| MX2 \| 1.44 \| DISEASES 10763 \| NES \| 1.93 \| DISEASES 4763 \| NF1 \| 1.368 \| DISEASES 4782 \| NFIC \| 1.261 \| DISEASES 4938 \| OAS1 \| 1.54 \| DISEASES 5287 \| PIK3C2B \| 2.13 \| DISEASES 5447 \| POR \| 1.658 \| DISEASES 5728 \| PTEN \| 2.371 \| DISEASES 5270 \| SERPINE2 \| 1.177 \| DISEASES 6510 \| SLC1A5 \| 1.151 \| DISEASES 23583 \| SMUG1 \| 1.285 \| DISEASES 6657 \| SOX2 \| 2.427 \| DISEASES 200162 \| SPAG17 \| 1.72 \| DISEASES 161003 \| STOML3 \| 3.136 \| DISEASES 1678 \| TIMM8A \| 1.398 \| DISEASES 8771 \| TNFRSF6B \| 1.273 \| DISEASES 7187 \| TRAF3 \| 1.044 \| DISEASES 80036 \| TRPM3 \| 1.79 \| DISEASES 139596 \| UPRT \| 1.795 \| DISEASES 7422 \| VEGFA \| 1.214 \| DISEASES
Locus	Symbol \| Locus(Total Locus:12) NFKBIA \| 14q13.2 SEPT14 \| 7p11.2 LZTR1 \| 22q11.21 EGFR \| 7p11.2 TP53 \| 17p13.1 FGFR3 \| 4p16.3 PPARG \| 3p25.2 TACC1 \| 8p11.22 MGMT \| 10q26.3 TACC3 \| 4p16.3 FGFR1 \| 8p11.23 IDH1 \| 2q34

Disease ID	1509
Disease	gliosarcoma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:7) HP:0004948 \| Twisted blood vessels \| 1 HP:0002859 \| Rhabdomyosarcoma \| 1 HP:0006779 \| Alveolar rhabdomyosarcoma \| 1 HP:0030065 \| Primitive neuroectodermal tumor \| 1 HP:0009733 \| Glioma \| 1 HP:0001510 \| Growth deficiency \| 1 HP:0002664 \| Neoplasia \| 1

Disease ID	1509
Disease	gliosarcoma
Manually Symptom	(Waiting for update.)
Text Mined Symptom	(Waiting for update.)

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Disease ID	1509
Disease	gliosarcoma
Case	(Waiting for update.)

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