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PedAM

Pediatric Disease Annotations & Medicines



   mucinous adenocarcinoma
  

Disease ID 1281
Disease mucinous adenocarcinoma
Definition
An adenocarcinoma producing mucin in significant amounts. (From Dorland, 27th ed)
Synonym
adenocarcinoma mucinous
adenocarcinoma mucous
adenocarcinoma, mucinous
adenocarcinoma, mucinous [disease/finding]
adenocarcinoma, mucinous, malignant
adenocarcinomas, mucinous
carcinoma, colloid
carcinoma, mucinous
carcinomas, colloid
carcinomas, mucinous
colloid adenocarcinoma
colloid carcinoma
colloid carcinomas
gelatinous adenocarcinoma
gelatinous carcinoma
mucinous adenocarcinoma (morphologic abnormality)
mucinous adenocarcinomas
mucinous carcinoma
mucinous carcinomas
mucoid adenocarcinoma
mucoid carcinoma
mucous adenocarcinoma
mucous carcinoma
pseudomyxoma peritonei with unknown primary site
DOID
UMLS
C0007130
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:19)
C0033822  |  pseudomyxoma peritonei  |  5
C0206696  |  signet ring cell carcinoma  |  3
C0011649  |  mature cystic teratoma  |  1
C0001418  |  adenocarcinoma  |  1
C0023601  |  leydig cell tumor  |  1
C0029401  |  paget's disease  |  1
C0001430  |  adenoma  |  1
C0039538  |  teratoma  |  1
C0007570  |  celiac disease  |  1
C0206723  |  sertoli-leydig cell tumor  |  1
C0334306  |  villous adenocarcinoma  |  1
C0031269  |  peutz-jeghers syndrome  |  1
C0206696  |  signet-ring cell carcinoma  |  1
C1334811  |  mucinous tumor  |  1
C0001418  |  adenocarcinomas  |  1
C0010631  |  cystadenocarcinoma  |  1
C0494165  |  liver metastasis  |  1
C1368903  |  cystic teratoma  |  1
C0205698  |  undifferentiated carcinoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
HOXD9  |  3235  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:128)
972  |  CD74  |  DISEASES
54474  |  KRT20  |  DISEASES
6793  |  STK10  |  DISEASES
51208  |  CLDN18  |  DISEASES
64090  |  GAL3ST2  |  DISEASES
2099  |  ESR1  |  DISEASES
1113  |  CHGA  |  DISEASES
27294  |  DHDH  |  DISEASES
1048  |  CEACAM5  |  DISEASES
2026  |  ENO2  |  DISEASES
51053  |  GMNN  |  DISEASES
4292  |  MLH1  |  DISEASES
4436  |  MSH2  |  DISEASES
2956  |  MSH6  |  DISEASES
7844  |  RNF103  |  DISEASES
9479  |  MAPK8IP1  |  DISEASES
4246  |  SCGB2A1  |  DISEASES
4738  |  NEDD8  |  DISEASES
3852  |  KRT5  |  DISEASES
9476  |  NAPSA  |  DISEASES
3845  |  KRAS  |  DISEASES
55333  |  SYNJ2BP  |  DISEASES
83998  |  REG4  |  DISEASES
57498  |  KIDINS220  |  DISEASES
10643  |  IGF2BP3  |  DISEASES
23314  |  SATB2  |  DISEASES
999  |  CDH1  |  DISEASES
6855  |  SYP  |  DISEASES
25884  |  CHRDL2  |  DISEASES
5290  |  PIK3CA  |  DISEASES
64374  |  SIL1  |  DISEASES
5395  |  PMS2  |  DISEASES
463  |  ZFHX3  |  DISEASES
284086  |  NEK8  |  DISEASES
7157  |  TP53  |  DISEASES
2064  |  ERBB2  |  DISEASES
10753  |  CAPN9  |  DISEASES
23671  |  TMEFF2  |  DISEASES
1956  |  EGFR  |  DISEASES
64434  |  NOM1  |  DISEASES
4249  |  MGAT5  |  DISEASES
9947  |  MAGEC1  |  DISEASES
6750  |  SST  |  DISEASES
3815  |  KIT  |  DISEASES
79623  |  GALNT14  |  DISEASES
5304  |  PIP  |  DISEASES
2672  |  GFI1  |  DISEASES
251  |  ALPPL2  |  DISEASES
7373  |  COL14A1  |  DISEASES
93210  |  PGAP3  |  DISEASES
4589  |  MUC7  |  DISEASES
11079  |  RER1  |  DISEASES
474  |  ATOH1  |  DISEASES
3171  |  FOXA3  |  DISEASES
54463  |  FAM134B  |  DISEASES
7275  |  TUB  |  DISEASES
9435  |  CHST2  |  DISEASES
89792  |  GAL3ST3  |  DISEASES
3265  |  HRAS  |  DISEASES
3172  |  HNF4A  |  DISEASES
354  |  KLK3  |  DISEASES
6844  |  VAMP2  |  DISEASES
2529  |  FUT7  |  DISEASES
4684  |  NCAM1  |  DISEASES
27436  |  EML4  |  DISEASES
923  |  CD6  |  DISEASES
5241  |  PGR  |  DISEASES
346389  |  MACC1  |  DISEASES
22906  |  TRAK1  |  DISEASES
3855  |  KRT7  |  DISEASES
23542  |  MAPK8IP2  |  DISEASES
10539  |  GLRX3  |  DISEASES
926  |  CD8B  |  DISEASES
9146  |  HGS  |  DISEASES
7490  |  WT1  |  DISEASES
2520  |  GAST  |  DISEASES
342035  |  GLDN  |  DISEASES
10948  |  STARD3  |  DISEASES
5269  |  SERPINB6  |  DISEASES
23583  |  SMUG1  |  DISEASES
23563  |  CHST5  |  DISEASES
8805  |  TRIM24  |  DISEASES
10164  |  CHST4  |  DISEASES
4089  |  SMAD4  |  DISEASES
921  |  CD5  |  DISEASES
1499  |  CTNNB1  |  DISEASES
22806  |  IKZF3  |  DISEASES
7080  |  NKX2-1  |  DISEASES
5979  |  RET  |  DISEASES
89122  |  TRIM4  |  DISEASES
3084  |  NRG1  |  DISEASES
1510  |  CTSE  |  DISEASES
6714  |  SRC  |  DISEASES
5116  |  PCNT  |  DISEASES
1999  |  ELF3  |  DISEASES
4311  |  MME  |  DISEASES
85414  |  SLC45A3  |  DISEASES
4582  |  MUC1  |  DISEASES
6098  |  ROS1  |  DISEASES
85413  |  SLC22A16  |  DISEASES
7422  |  VEGFA  |  DISEASES
729238  |  SFTPA2  |  DISEASES
25803  |  SPDEF  |  DISEASES
9314  |  KLF4  |  DISEASES
6520  |  SLC3A2  |  DISEASES
8434  |  RECK  |  DISEASES
2625  |  GATA3  |  DISEASES
444  |  ASPH  |  DISEASES
1045  |  CDX2  |  DISEASES
238  |  ALK  |  DISEASES
6370  |  CCL25  |  DISEASES
26269  |  FBXO8  |  DISEASES
307  |  ANXA4  |  DISEASES
51074  |  APIP  |  DISEASES
2120  |  ETV6  |  DISEASES
94025  |  MUC16  |  DISEASES
57614  |  KIAA1468  |  DISEASES
26960  |  NBEA  |  DISEASES
1029  |  CDKN2A  |  DISEASES
7849  |  PAX8  |  DISEASES
653509  |  SFTPA1  |  DISEASES
4588  |  MUC6  |  DISEASES
4583  |  MUC2  |  DISEASES
6513  |  SLC2A1  |  DISEASES
4585  |  MUC4  |  DISEASES
134145  |  FAM173B  |  DISEASES
4586  |  MUC5AC  |  DISEASES
727897  |  MUC5B  |  DISEASES
Locus(Waiting for update.)
Disease ID 1281
Disease mucinous adenocarcinoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:9)
HP:0002664  |  Neoplasia  |  6
HP:0010447  |  Fistula in ano  |  3
HP:0100570  |  Carcinoid tumor  |  3
HP:0000718  |  Aggressive behaviour  |  2
HP:0002608  |  Celiac disease  |  1
HP:0100590  |  Rectal fistula  |  1
HP:0030731  |  Carcinoma  |  1
HP:0001696  |  Situs inversus totalis  |  1
HP:0009792  |  Teratoma  |  1
Disease ID 1281
Disease mucinous adenocarcinoma
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms: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
rs11348802222522845673BRAFumls:C0007130BeFreeBRAF V600E mutation and CpG island methylation phenotype-positive status are similar in signet ring cell carcinoma and mucinous adenocarcinoma but more frequent when compared with conventional adenocarcinoma.0.0021715352012BRAF7140753336AT,G,C
rs121434568231433081956EGFRumls:C0007130BeFreeHere, we show that haploinsufficiency of Nkx2-1 in combination with oncogenic Kras(G12D), but not with oncogenic EGFR(L858R), caused pulmonary tumors in transgenic mice that were phenotypically similar to human mucinous adenocarcinomas.0.0050814512012EGFR755191822TG
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:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0007130diethylstilbestrolD00405456-53-1adenocarcinoma, mucinousMESH:D002288marker/mechanism7672708
C0007130fluorouracilD00547251-21-8adenocarcinoma, mucinousMESH:D002288marker/mechanism15228453
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)