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PedAM

Pediatric Disease Annotations & Medicines



   endodermal sinus tumor
  

Disease ID 1512
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
Disease endodermal sinus tumor
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:2)
HP:0100621  |  Dysgerminoma  |  1
HP:0005214  |  Bowel obstruction  |  1
Disease ID 1512
Disease endodermal sinus tumor
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:2)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs104894972108524656736SRYumls:C0014145BeFreeIdentification 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.0.0002714422000SRYY2787320CT
rs104894972108524656749SSRP1umls:C0014145BeFreeIdentification 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.0.0002714422000SRYY2787320CT
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.)
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)