endodermal sinus tumor |
Disease ID | 1512 |
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Disease | endodermal sinus tumor |
Definition | An unusual and aggressive tumor of germ-cell origin that reproduces the extraembryonic structures of the early embryo. It is the most common malignant germ cell tumor found in children. It is characterized by a labyrinthine glandular pattern of flat epithelial cells and rounded papillary processes with a central capillary (Schiller-Duval body). The tumor is rarely bilateral. Before the use of combination chemotherapy, the tumor was almost invariably fatal. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1189) |
Synonym | embryonal carcinoma, infantile endodermal sinus neoplasm endodermal sinus tumor (morphologic abnormality) endodermal sinus tumor [disease/finding] endodermal sinus tumors endodermal sinus tumour hepatoid yolk sac tumor hepatoid yolk sac tumour infantile embryonal carcinoma orchioblastoma polyvesicular vitelline tumor polyvesicular vitelline tumour tumor, endodermal sinus tumor, yolk sac tumors, endodermal sinus tumors, yolk sac yolk sac neoplasm yolk sac tumor yolk sac tumor (disorder) yolk sac tumor site unspecified yolk sac tumor, malignant yolk sac tumors yolk sac tumour yolk sac tumour site unspecified |
Orphanet | |
DOID | |
UMLS | C0014145 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:4) C0014145 | endodermal sinus tumor | 10 C0024291 | hemophagocytic syndrome | 1 C0013377 | dysgerminoma | 1 C0021843 | intestinal obstruction | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | (Waiting for update.) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:94) 64132 | XYLT2 | DISEASES 7022 | TFAP2C | DISEASES 3956 | LGALS1 | DISEASES 113791 | PIK3IP1 | DISEASES 57167 | SALL4 | DISEASES 10423 | CDIPT | DISEASES 1158 | CKM | DISEASES 1048 | CEACAM5 | DISEASES 7980 | TFPI2 | DISEASES 2026 | ENO2 | DISEASES 79923 | NANOG | DISEASES 55856 | ACOT13 | DISEASES 7276 | TTR | DISEASES 3217 | HOXB7 | DISEASES 79441 | HAUS3 | DISEASES 6662 | SOX9 | DISEASES 6939 | TCF15 | DISEASES 9476 | NAPSA | DISEASES 1160 | CKMT2 | DISEASES 4836 | NMT1 | DISEASES 5460 | POU5F1 | DISEASES 4072 | EPCAM | DISEASES 943 | TNFRSF8 | DISEASES 8034 | SLC25A16 | DISEASES 23598 | PATZ1 | DISEASES 7157 | TP53 | DISEASES 29947 | DNMT3L | DISEASES 10733 | PLK4 | DISEASES 10637 | LEFTY1 | DISEASES 6581 | SLC22A3 | DISEASES 23082 | PPRC1 | DISEASES 3815 | KIT | DISEASES 90737 | PAGE5 | DISEASES 251 | ALPPL2 | DISEASES 213 | ALB | DISEASES 6997 | TDGF1 | DISEASES 64321 | SOX17 | DISEASES 1152 | CKB | DISEASES 1159 | CKMT1B | DISEASES 794 | CALB2 | DISEASES 1442 | CSH1 | DISEASES 6664 | SOX11 | DISEASES 6657 | SOX2 | DISEASES 10494 | STK25 | DISEASES 3855 | KRT7 | DISEASES 4496 | MT1H | DISEASES 7490 | WT1 | DISEASES 9573 | GDF3 | DISEASES 668 | FOXL2 | DISEASES 2938 | GSTA1 | DISEASES 554 | AVPR2 | DISEASES 7704 | ZBTB16 | DISEASES 359787 | DPPA3 | DISEASES 5348 | FXYD1 | DISEASES 2100 | ESR2 | DISEASES 55107 | ANO1 | DISEASES 5265 | SERPINA1 | DISEASES 55124 | PIWIL2 | DISEASES 5802 | PTPRS | DISEASES 23224 | SYNE2 | DISEASES 2526 | FUT4 | DISEASES 4311 | MME | DISEASES 7044 | LEFTY2 | DISEASES 3142 | HLX | DISEASES 4751 | NEK2 | DISEASES 7259 | TSPYL1 | DISEASES 2516 | NR5A1 | DISEASES 2170 | FABP3 | DISEASES 94027 | CGB7 | DISEASES 1832 | DSP | DISEASES 1045 | CDX2 | DISEASES 1761 | DMRT1 | DISEASES 6736 | SRY | DISEASES 6370 | CCL25 | DISEASES 1443 | CSH2 | DISEASES 2719 | GPC3 | DISEASES 174 | AFP | DISEASES 221002 | RASGEF1A | DISEASES 8091 | HMGA2 | DISEASES 7018 | TF | DISEASES 9058 | SLC13A2 | DISEASES 2674 | GFRA1 | DISEASES 7849 | PAX8 | DISEASES 7258 | TSPY1 | DISEASES 94115 | CGB8 | DISEASES 284111 | SLC13A5 | DISEASES 100289087 | TSPY10 | DISEASES 548596 | CKMT1A | DISEASES 196527 | ANO6 | DISEASES 4585 | MUC4 | DISEASES 5099 | PCDH7 | DISEASES 3939 | LDHA | DISEASES 9212 | AURKB | DISEASES 732253 | TDRG1 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 1512 |
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Disease | endodermal sinus tumor |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:2) |
Disease ID | 1512 |
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Disease | endodermal sinus tumor |
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:2) | |||||||||||||
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snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
rs104894972 | 10852465 | 6736 | SRY | umls:C0014145 | BeFree | Identification of a new missense mutation (Gly95Glu) in a highly conserved codon within the high-mobility group box of the sex-determining region Y gene: report on a 46,XY female with gonadal dysgenesis and yolk-sac tumor. | 0.000271442 | 2000 | SRY | Y | 2787320 | C | T |
rs104894972 | 10852465 | 6749 | SSRP1 | umls:C0014145 | BeFree | Identification of a new missense mutation (Gly95Glu) in a highly conserved codon within the high-mobility group box of the sex-determining region Y gene: report on a 46,XY female with gonadal dysgenesis and yolk-sac tumor. | 0.000271442 | 2000 | SRY | Y | 2787320 | C | T |
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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