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PedAM

Pediatric Disease Annotations & Medicines



   cystadenoma
  

Disease ID 1540
Disease cystadenoma
Definition
A benign neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. In some instances, considerable portions of the neoplasm, or even the entire mass, may be cystic. (Stedman, 25th ed)
Synonym
[m]cystadenoma nos
cystadenoma (disorder)
cystadenoma (morphologic abnormality)
cystadenoma [disease/finding]
cystadenoma, benign
cystadenoma, nos
cystadenomas
cystoma, nos
DOID
UMLS
C0010633
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:34)
C0039538  |  teratoma  |  3
C0006160  |  brenner tumor  |  2
C0026684  |  appendiceal mucocele  |  2
C0033822  |  pseudomyxoma peritonei  |  1
C0206681  |  clear cell carcinoma  |  1
C0008340  |  congenital choledochal cyst  |  1
C0023798  |  lipoma  |  1
C0032987  |  ectopic pregnancy  |  1
C0010635  |  mucinous cystadenoma  |  1
C0008340  |  choledochal cyst  |  1
C0037274  |  skin disease  |  1
C0026684  |  mucocele of the appendix  |  1
C1368903  |  cystic teratoma  |  1
C0085113  |  neurofibromatosis  |  1
C0345893  |  juvenile polyposis  |  1
C0010631  |  cystadenocarcinoma  |  1
C0016045  |  fibroma  |  1
C0022354  |  obstructive jaundice  |  1
C0677886  |  ovarian epithelial cancer  |  1
C0021933  |  intussusception  |  1
C0021359  |  infertility  |  1
C0001418  |  adenocarcinoma  |  1
C0018206  |  granulosa cell tumor  |  1
C0269106  |  endosalpingiosis  |  1
C1261473  |  sarcoma  |  1
C0007137  |  squamous carcinoma  |  1
C0014175  |  endometriosis  |  1
C0019562  |  von hippel-lindau syndrome  |  1
C1335309  |  pancreatic mucinous cystadenoma  |  1
C0019562  |  von hippel-lindau disease  |  1
C0206623  |  adenosquamous carcinoma  |  1
C0879615  |  stromal tumor  |  1
C0019562  |  lindau disease  |  1
C0019562  |  hippel-lindau disease  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:114)
7544  |  ZFY  |  DISEASES
634  |  CEACAM1  |  DISEASES
3861  |  KRT14  |  DISEASES
54474  |  KRT20  |  DISEASES
51208  |  CLDN18  |  DISEASES
2099  |  ESR1  |  DISEASES
1113  |  CHGA  |  DISEASES
57167  |  SALL4  |  DISEASES
6880  |  TAF9  |  DISEASES
7249  |  TSC2  |  DISEASES
268  |  AMH  |  DISEASES
1048  |  CEACAM5  |  DISEASES
6528  |  SLC5A5  |  DISEASES
944  |  TNFSF8  |  DISEASES
657  |  BMPR1A  |  DISEASES
5216  |  PFN1  |  DISEASES
6928  |  HNF1B  |  DISEASES
64895  |  PAPOLG  |  DISEASES
3624  |  INHBA  |  DISEASES
3623  |  INHA  |  DISEASES
5589  |  PRKCSH  |  DISEASES
10343  |  PKDREJ  |  DISEASES
3845  |  KRAS  |  DISEASES
83998  |  REG4  |  DISEASES
5168  |  ENPP2  |  DISEASES
5460  |  POU5F1  |  DISEASES
5629  |  PROX1  |  DISEASES
5687  |  PSMA6  |  DISEASES
5934  |  RBL2  |  DISEASES
6855  |  SYP  |  DISEASES
5290  |  PIK3CA  |  DISEASES
10016  |  PDCD6  |  DISEASES
146862  |  UNC45B  |  DISEASES
432  |  ASGR1  |  DISEASES
7157  |  TP53  |  DISEASES
9869  |  SETDB1  |  DISEASES
201163  |  FLCN  |  DISEASES
760  |  CA2  |  DISEASES
3815  |  KIT  |  DISEASES
9669  |  EIF5B  |  DISEASES
3856  |  KRT8  |  DISEASES
1990  |  CELA1  |  DISEASES
6690  |  SPINK1  |  DISEASES
5245  |  PHB  |  DISEASES
3906  |  LALBA  |  DISEASES
4589  |  MUC7  |  DISEASES
5068  |  REG3A  |  DISEASES
794  |  CALB2  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
354  |  KLK3  |  DISEASES
6440  |  SFTPC  |  DISEASES
7156  |  TOP3A  |  DISEASES
6657  |  SOX2  |  DISEASES
5241  |  PGR  |  DISEASES
3855  |  KRT7  |  DISEASES
7490  |  WT1  |  DISEASES
2520  |  GAST  |  DISEASES
245908  |  DEFB105A  |  DISEASES
504180  |  DEFB105B  |  DISEASES
23436  |  CELA3B  |  DISEASES
51337  |  THEM6  |  DISEASES
10811  |  NOXA1  |  DISEASES
7316  |  UBC  |  DISEASES
7080  |  NKX2-1  |  DISEASES
55107  |  ANO1  |  DISEASES
8794  |  TNFRSF10C  |  DISEASES
160  |  AP2A1  |  DISEASES
4311  |  MME  |  DISEASES
23560  |  GTPBP4  |  DISEASES
3880  |  KRT19  |  DISEASES
3151  |  HMGN2  |  DISEASES
4582  |  MUC1  |  DISEASES
4288  |  MKI67  |  DISEASES
8661  |  EIF3A  |  DISEASES
8771  |  TNFRSF6B  |  DISEASES
10269  |  ZMPSTE24  |  DISEASES
5328  |  PLAU  |  DISEASES
57608  |  KIAA1462  |  DISEASES
4920  |  ROR2  |  DISEASES
778  |  CACNA1F  |  DISEASES
256297  |  PTF1A  |  DISEASES
4821  |  NKX2-2  |  DISEASES
22894  |  DIS3  |  DISEASES
768  |  CA9  |  DISEASES
9445  |  ITM2B  |  DISEASES
2592  |  GALT  |  DISEASES
7905  |  REEP5  |  DISEASES
2683  |  B4GALT1  |  DISEASES
1045  |  CDX2  |  DISEASES
192668  |  CYS1  |  DISEASES
6736  |  SRY  |  DISEASES
2878  |  GPX3  |  DISEASES
3875  |  KRT18  |  DISEASES
6370  |  CCL25  |  DISEASES
12  |  SERPINA3  |  DISEASES
2719  |  GPC3  |  DISEASES
174  |  AFP  |  DISEASES
4338  |  MOCS2  |  DISEASES
23028  |  KDM1A  |  DISEASES
79744  |  ZNF419  |  DISEASES
9564  |  BCAR1  |  DISEASES
7849  |  PAX8  |  DISEASES
5076  |  PAX2  |  DISEASES
6304  |  SATB1  |  DISEASES
4588  |  MUC6  |  DISEASES
55898  |  UNC45A  |  DISEASES
4583  |  MUC2  |  DISEASES
85441  |  HELZ2  |  DISEASES
4585  |  MUC4  |  DISEASES
59351  |  PBOV1  |  DISEASES
4586  |  MUC5AC  |  DISEASES
374569  |  ASPG  |  DISEASES
283131  |  NEAT1  |  DISEASES
Locus(Waiting for update.)
Disease ID 1540
Disease cystadenoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:20)
HP:0002664  |  Neoplasia  |  14
HP:0009792  |  Teratoma  |  3
HP:0100615  |  Neoplasm of the ovary  |  2
HP:0012531  |  Pain  |  1
HP:0011962  |  Obstructive azoospermia  |  1
HP:0002576  |  Intussusception  |  1
HP:0030731  |  Carcinoma  |  1
HP:0002835  |  Aspiration  |  1
HP:0100890  |  Cyst of the ductus choledochus  |  1
HP:0010618  |  Ovarian fibroma  |  1
HP:0000952  |  Yellow skin  |  1
HP:0003418  |  Back pain  |  1
HP:0100242  |  Sarcoma  |  1
HP:0000789  |  Infertility  |  1
HP:0001067  |  Neurofibromas  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0030127  |  Endometriosis  |  1
HP:0100570  |  Carcinoid tumor  |  1
HP:0012032  |  Lipoma  |  1
HP:0010614  |  Fibroma  |  1
Disease ID 1540
Disease cystadenoma
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs3865450441682885011200CHEK2umls:C0010633BeFreePositive associations were seen with the CHEK2 I157T missense variant and ovarian cystadenomas (OR = 1.7; P = 0.005), with borderline ovarian cancers (OR = 2.6; P = 0.002) and with low-grade invasive cancers (OR = 2.1; P = 0.04).0.0002714422006NANANANANA
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:1)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0010633diethylstilbestrolD00405456-53-1cystadenomaMESH:D003537marker/mechanism165277
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)