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PedAM

Pediatric Disease Annotations & Medicines



   portal hypertension
  

Disease ID 327
Disease portal hypertension
Definition
Abnormal increase of resistance to blood flow within the hepatic PORTAL SYSTEM, frequently seen in LIVER CIRRHOSIS and conditions with obstruction of the PORTAL VEIN.
Synonym
hypertension portal
hypertension, portal
hypertension, portal [disease/finding]
hypertensions, portal
pht - portal hypertension
portal hypertension (disorder)
portal hypertensions
DOID
ICD10
UMLS
C0020541
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:121)
C0023890  |  cirrhosis  |  166
C0042345  |  varices  |  71
C0023890  |  liver cirrhosis  |  62
C0023895  |  liver disease  |  47
C0014867  |  esophageal varices  |  35
C0020532  |  hypersplenism  |  18
C0040053  |  thrombosis  |  14
C1619734  |  pulmonary arterial hypertension  |  12
C0014867  |  oesophageal varices  |  12
C0036323  |  schistosomiasis  |  11
C0023895  |  liver diseases  |  11
C0155773  |  portal vein thrombosis  |  10
C0020538  |  hypertension  |  8
C0019204  |  hepatocellular carcinoma  |  7
C0005411  |  biliary atresia  |  7
C0023890  |  hepatic cirrhosis  |  6
C0040034  |  thrombocytopenia  |  6
C0023891  |  alcoholic cirrhosis  |  6
C0019196  |  hepatitis c  |  5
C0008312  |  biliary cirrhosis  |  4
C0002871  |  anemia  |  4
C0030305  |  pancreatitis  |  4
C0036202  |  sarcoidosis  |  3
C0019158  |  hepatitis  |  3
C1260402  |  splenic sequestration  |  3
C0023895  |  hepatic disease  |  3
C0020542  |  pulmonary hypertension  |  3
C0155747  |  splenic artery aneurysm  |  3
C0024623  |  gastric cancer  |  3
C0001815  |  myelofibrosis  |  3
C0600452  |  hepatopulmonary syndrome  |  2
C0085413  |  autosomal dominant polycystic kidney  |  2
C0023418  |  leukemia  |  2
C0008340  |  choledochal cyst  |  2
C0085413  |  autosomal dominant polycystic kidney disease  |  2
C0018920  |  cavernoma  |  2
C0029454  |  osteopetrosis  |  2
C0030312  |  pancytopenia  |  2
C0019212  |  hepatorenal syndrome  |  2
C0023890  |  cirrhosis of liver  |  2
C0019151  |  hepatic encephalopathy  |  2
C0014848  |  achalasia  |  1
C0021390  |  inflammatory bowel disease  |  1
C0030781  |  peliosis hepatis  |  1
C1333977  |  hepatitis b virus-related hepatocellular carcinoma  |  1
C0013502  |  hydatid cyst  |  1
C0001815  |  idiopathic myelofibrosis  |  1
C1112746  |  hepatic lymphoma  |  1
C0494165  |  liver metastases  |  1
C0017658  |  glomerulonephritis  |  1
C0009782  |  connective tissue disease  |  1
C0241910  |  autoimmune hepatitis  |  1
C0002878  |  hemolytic anemia  |  1
C0085404  |  poems syndrome  |  1
C0042345  |  varicose veins  |  1
C0027947  |  neutropenia  |  1
C0023487  |  promyelocytic leukemia  |  1
C0019163  |  hepatitis b  |  1
C0023487  |  acute promyelocytic leukemia  |  1
C0021831  |  enteropathy  |  1
C0023470  |  myelocytic leukemia  |  1
C0023281  |  leishmaniasis  |  1
C0042345  |  varicosities  |  1
C0009402  |  colorectal cancer  |  1
C0023891  |  alcoholic liver cirrhosis  |  1
C0042373  |  vascular disorders  |  1
C0042373  |  vascular disease  |  1
C0024523  |  malabsorption  |  1
C0010674  |  cystic fibrosis  |  1
C0009319  |  colitis  |  1
C0024899  |  mastocytosis  |  1
C0023290  |  visceral leishmaniasis  |  1
C0003615  |  appendicitis  |  1
C0206754  |  neuroendocrine tumors  |  1
C0017205  |  gaucher's disease  |  1
C0007570  |  coeliac disease  |  1
C0007113  |  rectal cancer  |  1
C0002726  |  amyloidosis  |  1
C0221013  |  systemic mastocytosis  |  1
C0024299  |  lymphoma  |  1
C0036631  |  seminomas  |  1
C0019154  |  hepatic vein thrombosis  |  1
C0023895  |  hepatocellular disease  |  1
C0030286  |  pancreatic disease  |  1
C0008325  |  cholecystitis  |  1
C0018801  |  heart failure  |  1
C0162529  |  ischemic colitis  |  1
C0008311  |  cholangitis  |  1
C0019151  |  portosystemic encephalopathy  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0018916  |  hemangioma  |  1
C0018920  |  cavernous hemangioma  |  1
C0019187  |  alcoholic hepatitis  |  1
C0039445  |  hereditary hemorrhagic telangiectasia  |  1
C0042345  |  varicose vein  |  1
C0040147  |  thyroiditis  |  1
C0019322  |  umbilical hernia  |  1
C0162510  |  caroli disease  |  1
C0034150  |  peliosis  |  1
C0036319  |  schistosoma mansoni  |  1
C0677607  |  hashimoto's thyroiditis  |  1
C0085669  |  acute leukemia  |  1
C0027708  |  wilms' tumor  |  1
C0026272  |  mixed connective tissue disease  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0162316  |  iron deficiency anemia  |  1
C0699791  |  gastric carcinoma  |  1
C0019158  |  inflammatory liver disease  |  1
C0017152  |  gastritis  |  1
C0206754  |  neuroendocrine tumor  |  1
C0021831  |  bowel disease  |  1
C0149521  |  chronic pancreatitis  |  1
C0001430  |  adenoma  |  1
C0027022  |  myeloproliferative neoplasms  |  1
C0030286  |  pancreatic diseases  |  1
C0265965  |  dyskeratosis congenita  |  1
C0162429  |  poor nutrition  |  1
C0031154  |  peritonitis  |  1
C0007570  |  celiac disease  |  1
C0042373  |  vascular disorder  |  1
C0007222  |  cardiovascular disorders  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:3)
AVP  |  551  |  CTD_human
NOS3  |  4846  |  CTD_human
VEGFA  |  7422  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:239)
282706  |  DAOA-AS1  |  DISEASES
1080  |  CFTR  |  DISEASES
79657  |  RPAP3  |  DISEASES
10911  |  UTS2  |  DISEASES
84957  |  RELT  |  DISEASES
2249  |  FGF4  |  DISEASES
7066  |  THPO  |  DISEASES
25984  |  KRT23  |  DISEASES
3162  |  HMOX1  |  DISEASES
5834  |  PYGB  |  DISEASES
3929  |  LBP  |  DISEASES
27344  |  PCSK1N  |  DISEASES
7076  |  TIMP1  |  DISEASES
479  |  ATP12A  |  DISEASES
4313  |  MMP2  |  DISEASES
58189  |  WFDC1  |  DISEASES
3163  |  HMOX2  |  DISEASES
51285  |  RASL12  |  DISEASES
1512  |  CTSH  |  DISEASES
4051  |  CYP4F3  |  DISEASES
2091  |  FBL  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
9545  |  RAB3D  |  DISEASES
3082  |  HGF  |  DISEASES
5054  |  SERPINE1  |  DISEASES
55163  |  PNPO  |  DISEASES
1277  |  COL1A1  |  DISEASES
1610  |  DAO  |  DISEASES
64895  |  PAPOLG  |  DISEASES
4852  |  NPY  |  DISEASES
64105  |  CENPK  |  DISEASES
1948  |  EFNB2  |  DISEASES
56914  |  OTOR  |  DISEASES
6945  |  MLX  |  DISEASES
10365  |  KLF2  |  DISEASES
2678  |  GGT1  |  DISEASES
54567  |  DLL4  |  DISEASES
3630  |  INS  |  DISEASES
2006  |  ELN  |  DISEASES
5589  |  PRKCSH  |  DISEASES
59272  |  ACE2  |  DISEASES
1571  |  CYP2E1  |  DISEASES
10343  |  PKDREJ  |  DISEASES
2161  |  F12  |  DISEASES
8431  |  NR0B2  |  DISEASES
23225  |  NUP210  |  DISEASES
5791  |  PTPRE  |  DISEASES
1401  |  CRP  |  DISEASES
187  |  APLNR  |  DISEASES
3569  |  IL6  |  DISEASES
9394  |  HS6ST1  |  DISEASES
255488  |  RNF144B  |  DISEASES
4659  |  PPP1R12A  |  DISEASES
7450  |  VWF  |  DISEASES
4223  |  MEOX2  |  DISEASES
6521  |  SLC4A1  |  DISEASES
495  |  ATP4A  |  DISEASES
7077  |  TIMP2  |  DISEASES
2549  |  GAB1  |  DISEASES
3553  |  IL1B  |  DISEASES
8726  |  EED  |  DISEASES
6403  |  SELP  |  DISEASES
8647  |  ABCB11  |  DISEASES
3791  |  KDR  |  DISEASES
57514  |  ARHGAP31  |  DISEASES
590  |  BCHE  |  DISEASES
80725  |  SRCIN1  |  DISEASES
2162  |  F13A1  |  DISEASES
3827  |  KNG1  |  DISEASES
80315  |  CPEB4  |  DISEASES
5244  |  ABCB4  |  DISEASES
409  |  ARRB2  |  DISEASES
432  |  ASGR1  |  DISEASES
207  |  AKT1  |  DISEASES
2702  |  GJA5  |  DISEASES
5972  |  REN  |  DISEASES
185  |  AGTR1  |  DISEASES
167410  |  LIX1  |  DISEASES
2041  |  EPHA1  |  DISEASES
3439  |  IFNA1  |  DISEASES
133  |  ADM  |  DISEASES
1360  |  CPB1  |  DISEASES
5205  |  ATP8B1  |  DISEASES
23576  |  DDAH1  |  DISEASES
2776  |  GNAQ  |  DISEASES
6750  |  SST  |  DISEASES
1636  |  ACE  |  DISEASES
5739  |  PTGIR  |  DISEASES
5152  |  PDE9A  |  DISEASES
57572  |  DOCK6  |  DISEASES
4880  |  NPPC  |  DISEASES
285203  |  EOGT  |  DISEASES
213  |  ALB  |  DISEASES
54859  |  ELP6  |  DISEASES
327  |  APEH  |  DISEASES
116379  |  IL22RA2  |  DISEASES
4846  |  NOS3  |  DISEASES
203286  |  ANKS6  |  DISEASES
8642  |  DCHS1  |  DISEASES
94274  |  PPP1R14A  |  DISEASES
3479  |  IGF1  |  DISEASES
59350  |  RXFP1  |  DISEASES
8862  |  APLN  |  DISEASES
2353  |  FOS  |  DISEASES
4968  |  OGG1  |  DISEASES
6373  |  CXCL11  |  DISEASES
9451  |  EIF2AK3  |  DISEASES
2147  |  F2  |  DISEASES
5340  |  PLG  |  DISEASES
6868  |  ADAM17  |  DISEASES
947  |  CD34  |  DISEASES
27257  |  LSM1  |  DISEASES
358  |  AQP1  |  DISEASES
118430  |  MUCL1  |  DISEASES
80169  |  CTC1  |  DISEASES
1909  |  EDNRA  |  DISEASES
9475  |  ROCK2  |  DISEASES
6014  |  RIT2  |  DISEASES
3039  |  HBA1  |  DISEASES
8706  |  B3GALNT1  |  DISEASES
2837  |  UTS2R  |  DISEASES
9622  |  KLK4  |  DISEASES
117584  |  RFFL  |  DISEASES
4843  |  NOS2  |  DISEASES
147719  |  LYPD4  |  DISEASES
286826  |  LIN9  |  DISEASES
286753  |  TUSC5  |  DISEASES
527  |  ATP6V0C  |  DISEASES
7490  |  WT1  |  DISEASES
2520  |  GAST  |  DISEASES
6297  |  SALL2  |  DISEASES
2152  |  F3  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
957  |  ENTPD5  |  DISEASES
10957  |  PNRC1  |  DISEASES
1908  |  EDN3  |  DISEASES
3988  |  LIPA  |  DISEASES
4842  |  NOS1  |  DISEASES
3363  |  HTR7  |  DISEASES
3266  |  ERAS  |  DISEASES
857  |  CAV1  |  DISEASES
4128  |  MAOA  |  DISEASES
10164  |  CHST4  |  DISEASES
6672  |  SP100  |  DISEASES
2701  |  GJA4  |  DISEASES
8654  |  PDE5A  |  DISEASES
5265  |  SERPINA1  |  DISEASES
84458  |  LCOR  |  DISEASES
6288  |  SAA1  |  DISEASES
6752  |  SSTR2  |  DISEASES
2050  |  EPHB4  |  DISEASES
1969  |  EPHA2  |  DISEASES
9583  |  ENTPD4  |  DISEASES
9332  |  CD163  |  DISEASES
4478  |  MSN  |  DISEASES
26580  |  BSCL2  |  DISEASES
5742  |  PTGS1  |  DISEASES
4283  |  CXCL9  |  DISEASES
5321  |  PLA2G4A  |  DISEASES
5743  |  PTGS2  |  DISEASES
462  |  SERPINC1  |  DISEASES
1490  |  CTGF  |  DISEASES
55974  |  SLC50A1  |  DISEASES
85413  |  SLC22A16  |  DISEASES
1268  |  CNR1  |  DISEASES
959  |  CD40LG  |  DISEASES
7803  |  PTP4A1  |  DISEASES
1491  |  CTH  |  DISEASES
79819  |  WDR78  |  DISEASES
5314  |  PKHD1  |  DISEASES
5950  |  RBP4  |  DISEASES
8813  |  DPM1  |  DISEASES
11253  |  MAN1B1  |  DISEASES
11093  |  ADAMTS13  |  DISEASES
7422  |  VEGFA  |  DISEASES
4318  |  MMP9  |  DISEASES
4352  |  MPL  |  DISEASES
1025  |  CDK9  |  DISEASES
84890  |  ADO  |  DISEASES
659  |  BMPR2  |  DISEASES
2155  |  F7  |  DISEASES
57819  |  LSM2  |  DISEASES
23564  |  DDAH2  |  DISEASES
3055  |  HCK  |  DISEASES
4524  |  MTHFR  |  DISEASES
7056  |  THBD  |  DISEASES
1910  |  EDNRB  |  DISEASES
3274  |  HRH2  |  DISEASES
64344  |  HIF3A  |  DISEASES
688  |  KLF5  |  DISEASES
1906  |  EDN1  |  DISEASES
3096  |  HIVEP1  |  DISEASES
3704  |  ITPA  |  DISEASES
551  |  AVP  |  DISEASES
3030  |  HADHA  |  DISEASES
56897  |  WRNIP1  |  DISEASES
3717  |  JAK2  |  DISEASES
3875  |  KRT18  |  DISEASES
94  |  ACVRL1  |  DISEASES
51070  |  NOSIP  |  DISEASES
29994  |  BAZ2B  |  DISEASES
51466  |  EVL  |  DISEASES
54903  |  MKS1  |  DISEASES
51520  |  LARS  |  DISEASES
91807  |  MYLK3  |  DISEASES
6696  |  SPP1  |  DISEASES
174  |  AFP  |  DISEASES
655  |  BMP7  |  DISEASES
728441  |  GGT2  |  DISEASES
1363  |  CPE  |  DISEASES
64881  |  PCDH20  |  DISEASES
2641  |  GCG  |  DISEASES
8671  |  SLC4A4  |  DISEASES
388552  |  BLOC1S3  |  DISEASES
115677  |  NOSTRIN  |  DISEASES
23210  |  JMJD6  |  DISEASES
55683  |  KANSL3  |  DISEASES
7124  |  TNF  |  DISEASES
387  |  RHOA  |  DISEASES
5817  |  PVR  |  DISEASES
9498  |  SLC4A8  |  DISEASES
3276  |  PRMT1  |  DISEASES
408  |  ARRB1  |  DISEASES
3586  |  IL10  |  DISEASES
6434  |  TRA2B  |  DISEASES
3077  |  HFE  |  DISEASES
284  |  ANGPT1  |  DISEASES
151306  |  GPBAR1  |  DISEASES
5333  |  PLCD1  |  DISEASES
55331  |  ACER3  |  DISEASES
84667  |  HES7  |  DISEASES
9971  |  NR1H4  |  DISEASES
5228  |  PGF  |  DISEASES
27229  |  TUBGCP4  |  DISEASES
64506  |  CPEB1  |  DISEASES
9294  |  S1PR2  |  DISEASES
100316868  |  HOTTIP  |  DISEASES
100506195  |  LARGE-AS1  |  DISEASES
Locus(Waiting for update.)
Disease ID 327
Disease portal hypertension
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:102)
HP:0001394  |  Hepatic cirrhosis  |  162
HP:0001541  |  Ascites  |  36
HP:0002584  |  Intestinal hemorrhage  |  35
HP:0001744  |  Splenomegaly  |  35
HP:0002239  |  Gastrointestinal hemorrhage  |  33
HP:0001971  |  Hypersplenism  |  18
HP:0030242  |  Blood clot in portal vein  |  10
HP:0001399  |  Liver failure  |  10
HP:0030731  |  Carcinoma  |  9
HP:0000822  |  Hypertension  |  8
HP:0005912  |  Biliary duct atresia  |  7
HP:0001402  |  Hepatocellular carcinoma  |  7
HP:0001395  |  Hepatic fibrosis  |  6
HP:0001410  |  Decreased liver function  |  6
HP:0006580  |  Portal fibrosis  |  6
HP:0001873  |  Low platelet count  |  6
HP:0001298  |  Encephalopathy  |  5
HP:0002092  |  Pulmonary artery hypertension  |  4
HP:0001903  |  Anemia  |  4
HP:0002613  |  Biliary cirrhosis  |  4
HP:0004947  |  Arteriovenous fistula  |  4
HP:0002617  |  Aneurysmal dilatation  |  4
HP:0000952  |  Yellow skin  |  4
HP:0012115  |  Liver inflammation  |  3
HP:0000790  |  Hematuria  |  3
HP:0000969  |  Dropsy  |  3
HP:0001405  |  Periportal fibrosis  |  3
HP:0001433  |  Enlarged liver and spleen  |  3
HP:0012126  |  Gastric cancer  |  3
HP:0001733  |  Pancreatic inflammation  |  3
HP:0001876  |  Low blood cell count  |  2
HP:0011002  |  Osteopetrosis  |  2
HP:0200123  |  Chronic liver inflammation  |  2
HP:0011974  |  Myelofibrosis  |  2
HP:0002202  |  Pleural effusion  |  2
HP:0001635  |  Congestive heart failure  |  2
HP:0002240  |  Enlarged liver  |  2
HP:0001909  |  Leukemia  |  2
HP:0001397  |  Hepatic steatosis  |  2
HP:0001747  |  Accessory spleen  |  2
HP:0004936  |  Blood clot in vein  |  2
HP:0002248  |  Vomitting blood  |  2
HP:0002480  |  Hepatic encephalopathy  |  2
HP:0012418  |  Low blood oxygen level  |  2
HP:0100890  |  Cyst of the ductus choledochus  |  2
HP:0100790  |  Hernia  |  2
HP:0002612  |  Congenital hepatic fibrosis  |  2
HP:0012587  |  Gross hematuria  |  1
HP:0001891  |  Iron-deficiency anemia  |  1
HP:0001048  |  Cavernous angioma  |  1
HP:0012649  |  Increased inflammatory response  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0000099  |  Glomerular nephritis  |  1
HP:0002583  |  Colitis  |  1
HP:0005263  |  Gastritis  |  1
HP:0011954  |  Nodular transformation of liver  |  1
HP:0002586  |  Peritonitis  |  1
HP:0001875  |  Neutropenia  |  1
HP:0001892  |  Bleeding diathesis  |  1
HP:0005225  |  Intestinal edema  |  1
HP:0002024  |  Intestinal malabsorption  |  1
HP:0002665  |  Lymphoma  |  1
HP:0000855  |  Insulin resistance  |  1
HP:0012223  |  Ruptured spleen  |  1
HP:0002608  |  Celiac disease  |  1
HP:0002573  |  Bloody diarrhea  |  1
HP:0002619  |  Varicose veins  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0001978  |  Extramedullary hematopoiesis  |  1
HP:0100033  |  Tic disorder  |  1
HP:0006577  |  Macronodular cirrhosis  |  1
HP:0002664  |  Neoplasia  |  1
HP:0003256  |  Coagulopathy  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0100699  |  Scarring  |  1
HP:0002910  |  Elevated transaminases  |  1
HP:0002571  |  Achalasia  |  1
HP:0012281  |  Chylous ascites  |  1
HP:0100844  |  Pancreatic fistula  |  1
HP:0100626  |  Chronic hepatic failure  |  1
HP:0030151  |  Cholangitis  |  1
HP:0004836  |  Acute promyelocytic leukemia  |  1
HP:0100646  |  Thyroiditis  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
HP:0012550  |  Colonic varices  |  1
HP:0012849  |  Small intestinal hemorrhage  |  1
HP:0012378  |  Fatigue  |  1
HP:0002242  |  Enteropathy  |  1
HP:0100495  |  Mastocytosis  |  1
HP:0001537  |  Umbilical hernias  |  1
HP:0001082  |  Cholecystitis  |  1
HP:0006280  |  Chronic pancreas inflammation  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0011034  |  Amyloid disease  |  1
HP:0030243  |  Blood clot in liver vein  |  1
HP:0001028  |  Strawberry mark  |  1
HP:0100806  |  Sepsis  |  1
HP:0012280  |  Hepatic amyloidosis  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0002488  |  Acute leukemias  |  1
HP:0030247  |  Blood clot in splanchnic vein  |  1
Disease ID 327
Disease portal hypertension
Manually Symptom
UMLS  | Name(Total Manually Symptoms:117)
C2707258  |  infections
C2676454  |  h syndrome
C2609100  |  anorectal varices
C2364133  |  infection
C2363955  |  venous reflux
C2243088  |  hemorrhagic gastritis
C2243088  |  haemorrhagic gastritis
C2073625  |  pleural effusion
C1963935  |  intestinal hyperemia
C1963854  |  congestive gastropathy
C1963220  |  pulmonary hypertension
C1963106  |  esophagitis
C1963101  |  encephalopathy
C1963091  |  diarrhea
C1868851  |  portopulmonary hypertension
C1657109  |  general problem
C1627365  |  littoral cell angioma
C1623038  |  cirrhosis
C1619734  |  pulmonary arterial hypertension
C1550639  |  fistula
C1442984  |  choledochal cyst
C1402315  |  vascular lesions
C1142158  |  hepatic vein occlusion
C1112565  |  pneumatosis intestinalis
C0947622  |  gallstones
C0941011  |  hemorrhagic gastropathy
C0877686  |  colopathy
C0856169  |  endothelial dysfunction
C0854441  |  gastric mucosal lesion
C0854416  |  pulmonary vascular disorders
C0796095  |  c syndrome
C0748168  |  pulmonary pathology
C0748159  |  pulmonary involvement
C0740577  |  acute abdominal pain
C0600452  |  hepatopulmonary syndrome
C0580178  |  duodenal varices
C0580174  |  portal hypertensive gastropathy
C0426768  |  o sign
C0376293  |  stigmata
C0348893  |  chronic superficial gastritis
C0341608  |  stomal varices
C0341244  |  duodenal erosion
C0333494  |  phlebosclerosis
C0267789  |  mesenteric arteriovenous fistula
C0267373  |  intestinal hemorrhages
C0267373  |  intestinal hemorrhage
C0267373  |  intestinal haemorrhages
C0267373  |  intestinal haemorrhage
C0267373  |  intestinal bleeding
C0267211  |  gastric antral vascular ectasia
C0267209  |  bleeding gastric varices
C0266807  |  acute gastrointestinal haemorrhage
C0266807  |  acute gastrointestinal bleeding
C0240318  |  mediastinal mass
C0238293  |  osteomyelosclerosis
C0235982  |  stricture of bile duct
C0235325  |  gastric hemorrhage
C0235325  |  gastric haemorrhage
C0235325  |  gastric bleeding
C0162529  |  ischemic colitis
C0162529  |  colonic ischemia
C0155789  |  esophageal varices hemorrhage
C0155789  |  bleeding oesophageal varices
C0155789  |  bleeding esophageal varices
C0155773  |  portal vein thrombosis
C0155747  |  splenic artery aneurysm
C0154307  |  congestive splenomegaly
C0152171  |  primary pulmonary hypertension
C0085584  |  encephalopathies
C0085113  |  von recklinghausen disease
C0042345  |  varicosities
C0042345  |  varicose veins
C0042345  |  varices
C0042341  |  varicocele
C0041296  |  tuberculosis
C0040034  |  thrombocytopenia
C0040028  |  hemorrhagic thrombocythemia
C0038358  |  gastric ulcer
C0038354  |  gastropathy
C0038354  |  gastric disease
C0032227  |  pleural effusions
C0030920  |  peptic ulcers
C0030920  |  peptic ulceration
C0030920  |  peptic ulcer
C0030920  |  gastroduodenal ulcer
C0024633  |  mallory-weiss syndrome
C0024620  |  primary liver cancer
C0024115  |  pulmonary disorders
C0023895  |  hepatocellular disease
C0023890  |  liver cirrhosis
C0020649  |  hypotension
C0020625  |  hyponatremia
C0020538  |  systemic arterial hypertension
C0020532  |  hypersplenism
C0020514  |  hyperprolactinemia
C0020488  |  sodium retention
C0019214  |  hepatosplenomegaly
C0019151  |  portal-systemic encephalopathy
C0019151  |  hepatic encephalopathy
C0019080  |  hemorrhage
C0019079  |  hemoptysis
C0018926  |  hematemesis
C0018926  |  haematemesis
C0018920  |  cavernous hemangioma
C0018920  |  cavernoma
C0017661  |  iga nephropathy
C0017205  |  gaucher's disease
C0017181  |  gastrointestinal hemorrhage
C0017145  |  gastric varix
C0017145  |  gastric varices
C0014867  |  oesophageal varices
C0014867  |  esophageal varices
C0008732  |  chylous ascites
C0008350  |  cholelithiasis
C0004936  |  mental disorders
C0002940  |  aneurysms
C0002940  |  aneurysm
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:51)
C0023890  |  cirrhosis  |  136
C0042345  |  varices  |  69
C0023890  |  liver cirrhosis  |  43
C0267373  |  intestinal bleeding  |  32
C0014867  |  esophageal varices  |  30
C0020532  |  hypersplenism  |  18
C0019080  |  hemorrhage  |  16
C0426768  |  o sign  |  15
C0017145  |  gastric varices  |  13
C1619734  |  pulmonary arterial hypertension  |  11
C0155773  |  portal vein thrombosis  |  10
C0040034  |  thrombocytopenia  |  6
C0016169  |  fistula  |  5
C0085584  |  encephalopathy  |  5
C0009450  |  infection  |  4
C0014867  |  oesophageal varices  |  4
C0017181  |  gastrointestinal hemorrhage  |  3
C0155747  |  splenic artery aneurysm  |  3
C0019214  |  hepatosplenomegaly  |  3
C0020542  |  pulmonary hypertension  |  3
C0856169  |  endothelial dysfunction  |  3
C0267373  |  intestinal hemorrhage  |  3
C0002940  |  aneurysm  |  2
C0018920  |  cavernoma  |  2
C0002940  |  aneurysms  |  2
C0032227  |  pleural effusion  |  2
C0018926  |  hematemesis  |  2
C0267209  |  bleeding gastric varices  |  2
C0019151  |  hepatic encephalopathy  |  2
C0008340  |  choledochal cyst  |  2
C0600452  |  hepatopulmonary syndrome  |  2
C0235325  |  gastric bleeding  |  1
C0877686  |  colopathy  |  1
C0023895  |  hepatocellular disease  |  1
C1868851  |  portopulmonary hypertension  |  1
C0162529  |  ischemic colitis  |  1
C0018920  |  cavernous hemangioma  |  1
C0042345  |  varicosities  |  1
C0854441  |  gastric mucosal lesion  |  1
C0018926  |  haematemesis  |  1
C0017205  |  gaucher's disease  |  1
C0008732  |  chylous ascites  |  1
C0042345  |  varicose veins  |  1
C0155789  |  bleeding esophageal varices  |  1
C0155789  |  bleeding oesophageal varices  |  1
C0580174  |  portal hypertensive gastropathy  |  1
C0038354  |  gastropathy  |  1
C0020625  |  hyponatremia  |  1
C0266807  |  acute gastrointestinal bleeding  |  1
C0748159  |  pulmonary involvement  |  1
C0341608  |  stomal varices  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:3)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1799945114211053077HFEumls:C0020541BeFreeWe describe here a kindred in which the propositus, being heterozygote for beta-thalassemia and the H63D mutation of the HFE gene, developed severe iron overload and in turn, chronic liver failure with portal hypertension.0.0005428842001HFE626090951CG
rs1800562194400631636ACEumls:C0020541BeFreeA 57-year-old white woman had serum ferritin 793 ng/mL, HFE C282Y homozygosity, elevated serum angiotensin-converting enzyme (ACE) levels, 3+ hepatocyte iron, cirrhosis, hepatic granulomas, and portal hypertension.0.0031813582009HFE626092913GA
rs1800562194400633077HFEumls:C0020541BeFreeA 57-year-old white woman had serum ferritin 793 ng/mL, HFE C282Y homozygosity, elevated serum angiotensin-converting enzyme (ACE) levels, 3+ hepatocyte iron, cirrhosis, hepatic granulomas, and portal hypertension.0.0005428842009HFE626092913GA
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:10)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0020541busulfanD00206655-98-1hypertension, portalMESH:D006975marker/mechanism267281
C0020541glutathioneD00597870-18-8hypertension, portalMESH:D006975marker/mechanism15962377
C0020541methotrexateD0087271959/5/2hypertension, portalMESH:D006975marker/mechanism5695945
C0020541nitric oxideD00956910102-43-9hypertension, portalMESH:D006975marker/mechanism15962377
C0020541octreotideD01528283150-76-9hypertension, portalMESH:D006975therapeutic9930395
C0020541propranololD011433525-66-6hypertension, portalMESH:D006975therapeutic10197489
C0020541spironolactoneD0131481952/1/7hypertension, portalMESH:D006975therapeutic12385542
C0020541thalidomideD01379250-35-1hypertension, portalMESH:D006975therapeutic14687169
C0020541vitamin aD01480111103-57-4hypertension, portalMESH:D006975marker/mechanism10750659
C0020541zidovudineD01521530516-87-1hypertension, portalMESH:D006975marker/mechanism11556343
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)