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Pediatric Disease Annotations & Medicines



   angiosarcoma
  

Disease ID 330
Disease angiosarcoma
Definition
A rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. (Stedman, 25th ed)
Synonym
angiosarcoma (disorder)
angiosarcomas
haemangioendothelial sarcoma
haemangioendothelioma, malignant
haemangiosarcoma
hemangioendothelial sarcoma
hemangioendothelioma, malignant
hemangioendothelioma, malignant (morphologic abnormality)
hemangiosarcoma
hemangiosarcoma (morphologic abnormality)
hemangiosarcoma [disease/finding]
hemangiosarcoma, malignant
hemangiosarcomas
malignant angioendothelioma
malignant haemangioendothelioma
malignant hemangioendothelioma
Orphanet
DOID
UMLS
C0018923
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:43)
C0024236  |  lymphedema  |  4
C0153676  |  pulmonary metastases  |  4
C1261473  |  sarcoma  |  3
C0012739  |  disseminated intravascular coagulation  |  2
C0153676  |  lung metastasis  |  2
C0018916  |  hemangioma  |  2
C0040034  |  thrombocytopenia  |  2
C0007177  |  cardiac tamponade  |  2
C0031039  |  pericardial effusion  |  2
C0002871  |  anemia  |  2
C0153676  |  lung metastases  |  2
C0153676  |  pulmonary metastasis  |  2
C0008479  |  chondrosarcoma  |  1
C0013595  |  eczema  |  1
C0027830  |  neurofibroma  |  1
C0040137  |  thyroid nodule  |  1
C0022739  |  klippel-trenaunay-weber syndrome  |  1
C0205696  |  anaplastic carcinoma  |  1
C0029463  |  osteosarcoma  |  1
C0085113  |  neurofibromatosis  |  1
C0025202  |  melanoma  |  1
C1704423  |  congenital lymphedema  |  1
C0265965  |  dyskeratosis congenita  |  1
C0242379  |  lung cancer  |  1
C0002878  |  hemolytic anemia  |  1
C0023890  |  hepatic cirrhosis  |  1
C0206667  |  adrenocortical adenoma  |  1
C0007137  |  squamous cell carcinoma  |  1
C0023890  |  cirrhosis  |  1
C0006142  |  breast cancer  |  1
C0494165  |  hepatic metastasis  |  1
C0153687  |  skin metastases  |  1
C0494165  |  liver metastases  |  1
C0677607  |  hashimoto thyroiditis  |  1
C0017205  |  gaucher disease  |  1
C0205788  |  epithelioid hemangioma  |  1
C0012739  |  consumptive coagulopathy  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0494165  |  hepatic metastases  |  1
C0040053  |  thrombosis  |  1
C0751674  |  lymphangioleiomyomatosis  |  1
C0023269  |  leiomyosarcoma  |  1
C0553580  |  ewing sarcoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:18)
TP53  |  7157  |  CTD_human
MYC  |  4609  |  CTD_human
KDR  |  3791  |  CTD_human
JUN  |  3725  |  CTD_human
CCND1  |  595  |  CTD_human
HRAS  |  3265  |  CTD_human
VEGFA  |  7422  |  CTD_human
COL18A1  |  80781  |  CTD_human
CSF3  |  1440  |  CTD_human
FLT1  |  2321  |  CTD_human
CTNNB1  |  1499  |  CTD_human
KRAS  |  3845  |  CTD_human
TEK  |  7010  |  CTD_human
PLCG1  |  5335  |  CTD_human
PTPRB  |  5787  |  CTD_human
GJA4  |  2701  |  CTD_human
VEGFC  |  7424  |  CTD_human
ANGPT2  |  285  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:161)
54474  |  KRT20  |  DISEASES
4710  |  NDUFB4  |  DISEASES
6725  |  SRMS  |  DISEASES
7038  |  TG  |  DISEASES
1048  |  CEACAM5  |  DISEASES
3036  |  HAS1  |  DISEASES
8402  |  SLC25A11  |  DISEASES
3558  |  IL2  |  DISEASES
595  |  CCND1  |  DISEASES
4254  |  KITLG  |  DISEASES
2026  |  ENO2  |  DISEASES
4012  |  LNPEP  |  DISEASES
4656  |  MYOG  |  DISEASES
5335  |  PLCG1  |  DISEASES
55831  |  EMC3  |  DISEASES
57187  |  THOC2  |  DISEASES
3232  |  HOXD3  |  DISEASES
4654  |  MYOD1  |  DISEASES
968  |  CD68  |  DISEASES
3852  |  KRT5  |  DISEASES
1571  |  CYP2E1  |  DISEASES
55422  |  ZNF331  |  DISEASES
2670  |  GFAP  |  DISEASES
23558  |  WBP2  |  DISEASES
6754  |  SSTR4  |  DISEASES
3845  |  KRAS  |  DISEASES
10894  |  LYVE1  |  DISEASES
5156  |  PDGFRA  |  DISEASES
11014  |  KDELR2  |  DISEASES
4069  |  LYZ  |  DISEASES
7450  |  VWF  |  DISEASES
5629  |  PROX1  |  DISEASES
8140  |  SLC7A5  |  DISEASES
5159  |  PDGFRB  |  DISEASES
2324  |  FLT4  |  DISEASES
466  |  ATF1  |  DISEASES
1031  |  CDKN2C  |  DISEASES
8030  |  CCDC6  |  DISEASES
6855  |  SYP  |  DISEASES
3791  |  KDR  |  DISEASES
943  |  TNFRSF8  |  DISEASES
5290  |  PIK3CA  |  DISEASES
4162  |  MCAM  |  DISEASES
7531  |  YWHAE  |  DISEASES
2247  |  FGF2  |  DISEASES
29999  |  FSCN3  |  DISEASES
1616  |  DAXX  |  DISEASES
1213  |  CLTC  |  DISEASES
7157  |  TP53  |  DISEASES
150094  |  SIK1  |  DISEASES
207  |  AKT1  |  DISEASES
6423  |  SFRP2  |  DISEASES
1956  |  EGFR  |  DISEASES
57689  |  LRRC4C  |  DISEASES
90952  |  ESAM  |  DISEASES
7424  |  VEGFC  |  DISEASES
5805  |  PTS  |  DISEASES
5281  |  PIGF  |  DISEASES
2321  |  FLT1  |  DISEASES
10413  |  YAP1  |  DISEASES
84959  |  UBASH3B  |  DISEASES
7508  |  XPC  |  DISEASES
1436  |  CSF1R  |  DISEASES
3815  |  KIT  |  DISEASES
115584  |  SLC5A11  |  DISEASES
3856  |  KRT8  |  DISEASES
10630  |  PDPN  |  DISEASES
7047  |  TGM4  |  DISEASES
51705  |  EMCN  |  DISEASES
4665  |  NAB2  |  DISEASES
4775  |  NFATC3  |  DISEASES
9482  |  STX8  |  DISEASES
1901  |  S1PR1  |  DISEASES
26287  |  ANKRD2  |  DISEASES
23261  |  CAMTA1  |  DISEASES
794  |  CALB2  |  DISEASES
10589  |  DRAP1  |  DISEASES
3213  |  HOXB3  |  DISEASES
2147  |  F2  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
7030  |  TFE3  |  DISEASES
285  |  ANGPT2  |  DISEASES
115207  |  KCTD12  |  DISEASES
10956  |  OS9  |  DISEASES
3039  |  HBA1  |  DISEASES
121227  |  LRIG3  |  DISEASES
64764  |  CREB3L2  |  DISEASES
3855  |  KRT7  |  DISEASES
7490  |  WT1  |  DISEASES
126282  |  TNFAIP8L1  |  DISEASES
2152  |  F3  |  DISEASES
5787  |  PTPRB  |  DISEASES
29015  |  SLC43A3  |  DISEASES
23583  |  SMUG1  |  DISEASES
23193  |  GANAB  |  DISEASES
1978  |  EIF4EBP1  |  DISEASES
9623  |  TCL1B  |  DISEASES
1003  |  CDH5  |  DISEASES
378884  |  NHLRC1  |  DISEASES
55107  |  ANO1  |  DISEASES
5979  |  RET  |  DISEASES
5265  |  SERPINA1  |  DISEASES
135250  |  RAET1E  |  DISEASES
25913  |  POT1  |  DISEASES
9332  |  CD163  |  DISEASES
4151  |  MB  |  DISEASES
2157  |  F8  |  DISEASES
4311  |  MME  |  DISEASES
25937  |  WWTR1  |  DISEASES
2475  |  MTOR  |  DISEASES
800  |  CALD1  |  DISEASES
3880  |  KRT19  |  DISEASES
57165  |  GJC2  |  DISEASES
1380  |  CR2  |  DISEASES
5788  |  PTPRC  |  DISEASES
10763  |  NES  |  DISEASES
387119  |  CEP85L  |  DISEASES
6098  |  ROS1  |  DISEASES
3897  |  L1CAM  |  DISEASES
27063  |  ANKRD1  |  DISEASES
5728  |  PTEN  |  DISEASES
7422  |  VEGFA  |  DISEASES
5429  |  POLH  |  DISEASES
7075  |  TIE1  |  DISEASES
2022  |  ENG  |  DISEASES
546  |  ATRX  |  DISEASES
4303  |  FOXO4  |  DISEASES
2155  |  F7  |  DISEASES
7056  |  THBD  |  DISEASES
54206  |  ERRFI1  |  DISEASES
6461  |  SHB  |  DISEASES
4609  |  MYC  |  DISEASES
23279  |  NUP160  |  DISEASES
6497  |  SKI  |  DISEASES
7010  |  TEK  |  DISEASES
2315  |  MLANA  |  DISEASES
51378  |  ANGPT4  |  DISEASES
10568  |  SLC34A2  |  DISEASES
6624  |  FSCN1  |  DISEASES
3875  |  KRT18  |  DISEASES
238  |  ALK  |  DISEASES
12  |  SERPINA3  |  DISEASES
196410  |  METTL7B  |  DISEASES
51074  |  APIP  |  DISEASES
174  |  AFP  |  DISEASES
54664  |  TMEM106B  |  DISEASES
342900  |  LEUTX  |  DISEASES
5609  |  MAP2K7  |  DISEASES
7122  |  CLDN5  |  DISEASES
1029  |  CDKN2A  |  DISEASES
387836  |  CLEC2A  |  DISEASES
257415  |  FAM133B  |  DISEASES
2130  |  EWSR1  |  DISEASES
8842  |  PROM1  |  DISEASES
6513  |  SLC2A1  |  DISEASES
4193  |  MDM2  |  DISEASES
284  |  ANGPT1  |  DISEASES
7164  |  TPD52L1  |  DISEASES
7090  |  TLE3  |  DISEASES
100128252  |  ZNF667-AS1  |  DISEASES
Locus(Waiting for update.)
Disease ID 330
Disease angiosarcoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:48)
HP:0002664  |  Neoplasia  |  10
HP:0001004  |  Lymphatic obstruction  |  4
HP:0002584  |  Intestinal hemorrhage  |  3
HP:0100242  |  Sarcoma  |  3
HP:0002027  |  Abdominal pain  |  3
HP:0002239  |  Gastrointestinal hemorrhage  |  3
HP:0001028  |  Strawberry mark  |  2
HP:0030731  |  Carcinoma  |  2
HP:0003256  |  Coagulopathy  |  2
HP:0012531  |  Pain  |  2
HP:0001873  |  Low platelet count  |  2
HP:0005521  |  Disseminated intravascular coagulation  |  2
HP:0001903  |  Anemia  |  2
HP:0001698  |  Pericardial effusions  |  2
HP:0002721  |  Immunodeficiency  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0002105  |  Hemoptysis  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
HP:0001399  |  Liver failure  |  1
HP:0009726  |  Renal neoplasm  |  1
HP:0100723  |  Gastrointestinal stroma tumor  |  1
HP:0010783  |  Erythema  |  1
HP:0000964  |  Eczema  |  1
HP:0012223  |  Ruptured spleen  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0100243  |  Leiomyosarcoma  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0001289  |  Confusion  |  1
HP:0002240  |  Enlarged liver  |  1
HP:0003764  |  Naevus  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0006765  |  Chondrosarcoma  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0002835  |  Aspiration  |  1
HP:0011854  |  Hemoperitoneum  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0001974  |  Leukocytosis  |  1
HP:0100820  |  Glomerulopathy  |  1
HP:0001067  |  Neurofibromas  |  1
HP:0002669  |  Osteosarcoma  |  1
HP:0008256  |  Adrenocortical adenomas  |  1
HP:0002625  |  Blood clot in a deep vein  |  1
HP:0001394  |  Hepatic cirrhosis  |  1
HP:0002861  |  Melanoma  |  1
HP:0012254  |  Ewing's sarcoma  |  1
HP:0004947  |  Arteriovenous fistula  |  1
HP:0000282  |  Facial puffiness  |  1
HP:0000790  |  Hematuria  |  1
Disease ID 330
Disease angiosarcoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:13)
C1519670  |  tumor angiogenesis
C1261473  |  malignant mesenchymal tumour
C0740401  |  perforation of duodenal ulcer
C0282607  |  vascular tumors
C0263367  |  koebner phenomenon
C0238246  |  hemangioma of the liver
C0221025  |  kasabach-merritt syndrome
C0153676  |  pulmonary metastasis
C0153676  |  pulmonary metastases
C0040053  |  thrombosis
C0040034  |  thrombocytopenia
C0027030  |  myiasis
C0007177  |  cardiac tamponade
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:6)
C0153676  |  pulmonary metastases  |  3
C0153676  |  pulmonary metastasis  |  2
C0007177  |  cardiac tamponade  |  2
C0040034  |  thrombocytopenia  |  2
C0221025  |  kasabach-merritt syndrome  |  2
C0040053  |  thrombosis  |  1
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
rs1764391207059542701GJA4umls:C0018923BeFreeA polymorphism in the human connexin37 (Cx37) gene (C1019T), resulting in a non-conservative amino acid change in the regulatory C-terminus (CT) of the Cx37 protein (P319S) has been suggested to be implicated in predisposition to angiosarcomas.0.1205428842010GJA4;LOC105378643134795168CT
rs56302315256790623791KDRumls:C0018923BeFreeLikewise, activating mutations in the receptor tyrosine kinase KDR (VEGFR2) have been reported in angiosarcomas and non-small cell lung cancers; the KDR A1065T mutation is reported to be sensitive to VEGFR kinase inhibitors, and fibroblast growth factor receptor inhibitors are in trials.0.1210857672015KDR455089802CT
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:5)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0018923diethylstilbestrolD00405456-53-1hemangiosarcomaMESH:D006394marker/mechanism567256
C0018923paclitaxelD017239-hemangiosarcomaMESH:D006394therapeutic9774950
C0018923peginterferon alfa-2bC417083-hemangiosarcomaMESH:D006394therapeutic15692506
C0018923pregabalinD000069583-hemangiosarcomaMESH:D006394marker/mechanism22539615
C0018923troglitazoneC05769397322-87-7hemangiosarcomaMESH:D006394marker/mechanism17569031
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)