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Pediatric Disease Annotations & Medicines



   budd-chiari syndrome
  

Disease ID 33
Disease budd-chiari syndrome
Definition
An obstruction in the veins of the liver caused by a blood clot (thrombosis). [HPO:probinson]
Synonym
blood clot in liver vein
budd chiari syndrome
budd chiari's syndrome
chiari syndrome
chiari syndromes
chiari's syndrome
hepatic vein obstruction
hepatic vein thromboses
hepatic vein thrombosis
hepatic vein thrombosis (disorder)
thromboses, hepatic vein
thrombosis, hepatic vein
vein thromboses, hepatic
vein thrombosis, hepatic
Orphanet
OMIM
DOID
ICD10
UMLS
C0019154
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:50)
C0019204  |  hepatocellular carcinoma  |  10
C0040053  |  thrombosis  |  7
C0004943  |  behcet's disease  |  5
C0948954  |  alveolar echinococcosis  |  3
C0023895  |  liver disease  |  3
C0836924  |  thrombocytosis  |  2
C0019048  |  hemoglobinuria  |  2
C0027022  |  myeloproliferative disorders  |  2
C0027022  |  myeloproliferative disorder  |  2
C0009319  |  colitis  |  2
C0009324  |  ulcerative colitis  |  2
C0024790  |  paroxysmal nocturnal hemoglobinuria  |  2
C0087086  |  thrombi  |  2
C0042345  |  varices  |  2
C0040053  |  thrombus  |  2
C0023487  |  acute promyelocytic leukaemia  |  1
C0009492  |  compartment syndrome  |  1
C0021831  |  bowel disease  |  1
C0035078  |  renal failure  |  1
C0346200  |  intravenous leiomyomatosis  |  1
C0007134  |  renal cell carcinoma  |  1
C0013502  |  hydatid cyst  |  1
C0019204  |  hepatocellular carcinomas  |  1
C0027022  |  myeloproliferative neoplasms  |  1
C0040034  |  thrombocytopenia  |  1
C0020541  |  portal hypertension  |  1
C0206654  |  leiomyomatosis  |  1
C0856761  |  hepatic vein obstruction  |  1
C1292778  |  chronic myeloproliferative disorders  |  1
C1377913  |  pleural mesothelioma  |  1
C1292778  |  chronic myeloproliferative disorder  |  1
C0398623  |  hypercoagulability  |  1
C0206141  |  hypereosinophilic syndrome  |  1
C0040028  |  essential thrombocytosis  |  1
C1334176  |  leiomyosarcoma of the inferior vena cava  |  1
C0022661  |  chronic renal failure  |  1
C0024790  |  paroxysmal nocturnal hemoglobinuria (pnh)  |  1
C0013502  |  echinococcosis  |  1
C0007570  |  celiac disease  |  1
C0334287  |  fibrolamellar hepatocellular carcinoma  |  1
C0878681  |  dent's disease  |  1
C0023890  |  liver cirrhosis  |  1
C0598608  |  hyperhomocysteinemia  |  1
C0021390  |  inflammatory bowel disease  |  1
C0004943  |  behcet disease  |  1
C0553980  |  endomyocardial fibrosis  |  1
C0023890  |  cirrhosis  |  1
C0600452  |  hepatopulmonary syndrome  |  1
C0040028  |  essential thrombocythemia  |  1
C0020538  |  hypertension  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:2)
F5  |  2153  |  ORPHANET
JAK2  |  3717  |  ORPHANET
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:5)
1559  |  CYP2C9  |  infer
2147  |  F2  |  infer
2153  |  F5  |  infer
2155  |  F7  |  infer
79001  |  VKORC1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:64)
1361  |  CPB2  |  DISEASES
350  |  APOH  |  DISEASES
3053  |  SERPIND1  |  DISEASES
10423  |  CDIPT  |  DISEASES
5327  |  PLAT  |  DISEASES
5054  |  SERPINE1  |  DISEASES
727  |  C5  |  DISEASES
2026  |  ENO2  |  DISEASES
7903  |  ST8SIA4  |  DISEASES
2161  |  F12  |  DISEASES
5156  |  PDGFRA  |  DISEASES
30061  |  SLC40A1  |  DISEASES
11019  |  LIAS  |  DISEASES
6558  |  SLC12A2  |  DISEASES
9739  |  SETD1A  |  DISEASES
443  |  ASPA  |  DISEASES
1  |  A1BG  |  DISEASES
79031  |  PDCL3  |  DISEASES
11107  |  PRDM5  |  DISEASES
7297  |  TYK2  |  DISEASES
178  |  AGL  |  DISEASES
2168  |  FABP1  |  DISEASES
213  |  ALB  |  DISEASES
27343  |  POLL  |  DISEASES
3094  |  HINT1  |  DISEASES
2147  |  F2  |  DISEASES
5340  |  PLG  |  DISEASES
6868  |  ADAM17  |  DISEASES
8884  |  SLC5A6  |  DISEASES
11037  |  STON1  |  DISEASES
1604  |  CD55  |  DISEASES
58492  |  ZNF77  |  DISEASES
811  |  CALR  |  DISEASES
2152  |  F3  |  DISEASES
81608  |  FIP1L1  |  DISEASES
3988  |  LIPA  |  DISEASES
966  |  CD59  |  DISEASES
132884  |  EVC2  |  DISEASES
3767  |  KCNJ11  |  DISEASES
2157  |  F8  |  DISEASES
462  |  SERPINC1  |  DISEASES
2153  |  F5  |  DISEASES
959  |  CD40LG  |  DISEASES
732  |  C8B  |  DISEASES
8813  |  DPM1  |  DISEASES
50945  |  TBX22  |  DISEASES
2155  |  F7  |  DISEASES
1184  |  CLCN5  |  DISEASES
4524  |  MTHFR  |  DISEASES
7056  |  THBD  |  DISEASES
57126  |  CD177  |  DISEASES
3704  |  ITPA  |  DISEASES
3030  |  HADHA  |  DISEASES
3717  |  JAK2  |  DISEASES
114899  |  C1QTNF3  |  DISEASES
83650  |  SLC35G5  |  DISEASES
174  |  AFP  |  DISEASES
56138  |  PCDHA11  |  DISEASES
1363  |  CPE  |  DISEASES
29072  |  SETD2  |  DISEASES
5817  |  PVR  |  DISEASES
133396  |  IL31RA  |  DISEASES
11075  |  STMN2  |  DISEASES
388588  |  SMIM1  |  DISEASES
Locus
Symbol | Locus(Total Locus:2)
JAK2  |  9p24.1
F5  |  1q24.2
Disease ID 33
Disease budd-chiari syndrome
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:18)
HP:0001082  |  Cholecystitis
HP:0001945  |  Fever
HP:0002240  |  Hepatomegaly
HP:0002910  |  Elevated hepatic transaminases
HP:0002239  |  Gastrointestinal hemorrhage
HP:0005214  |  Intestinal obstruction
HP:0001409  |  Portal hypertension
HP:0002586  |  Peritonitis
HP:0001824  |  Weight loss
HP:0001394  |  Cirrhosis
HP:0001744  |  Splenomegaly
HP:0000952  |  Jaundice
HP:0002024  |  Malabsorption
HP:0001541  |  Ascites
HP:0002040  |  Esophageal varix
HP:0002027  |  Abdominal pain
HP:0005244  |  Gastrointestinal infarctions
HP:0006554  |  Acute hepatic failure
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:27)
HP:0001402  |  Hepatocellular carcinoma  |  10
HP:0030731  |  Carcinoma  |  8
HP:0002583  |  Colitis  |  2
HP:0001399  |  Liver failure  |  2
HP:0001541  |  Ascites  |  2
HP:0005547  |  Myeloproliferative disorder  |  2
HP:0100279  |  Ulcerative colitis  |  2
HP:0004818  |  Paroxysmal nocturnal hemoglobinuria  |  2
HP:0004936  |  Blood clot in vein  |  2
HP:0001894  |  Thrombocytosis  |  2
HP:0003641  |  Hemoglobin in urine  |  2
HP:0100033  |  Tic disorder  |  2
HP:0001394  |  Hepatic cirrhosis  |  1
HP:0003270  |  Distended abdomen  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0006554  |  Acute hepatic failure  |  1
HP:0001409  |  Portal hypertension  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0001685  |  Myocardial fibrosis  |  1
HP:0002664  |  Neoplasia  |  1
HP:0002608  |  Celiac disease  |  1
HP:0000822  |  Hypertension  |  1
HP:0100002  |  Pleural mesothelioma  |  1
HP:0000952  |  Yellow skin  |  1
HP:0005584  |  Renal cell carcinoma  |  1
HP:0006685  |  Endocardial fibrosis  |  1
Disease ID 33
Disease budd-chiari syndrome
Manually Symptom
UMLS  | Name(Total Manually Symptoms:33)
C1963135  |  hepatic necrosis
C1861171  |  activated protein c resistance
C1512411  |  hepatocellular carcinoma
C1418558  |  paroxysmal nocturnal hemoglobinuria
C1402315  |  vascular lesions
C1285291  |  fetal ascites
C0600452  |  hepatopulmonary syndrome
C0584960  |  factor v leiden mutation
C0344688  |  patent ductus venosus
C0340757  |  inferior vena cava stenosis
C0267412  |  mesenteric thrombosis
C0266807  |  acute gastrointestinal bleeding
C0265072  |  inferior vena cava occlusion
C0265072  |  inferior vena cava obstruction
C0240225  |  hepatic mass
C0240066  |  iron deficiency
C0162557  |  fulminant hepatic failure
C0155773  |  portal vein thrombosis
C0040053  |  thrombosis
C0038833  |  superior vena cava obstruction
C0032463  |  polycythaemia vera
C0027022  |  myeloproliferative disorder
C0027022  |  myeloproliferative disease
C0026764  |  multiple myeloma
C0025202  |  malignant melanoma
C0023903  |  hepatoma
C0023890  |  liver cirrhosis
C0022665  |  tumor of the kidney
C0020639  |  hypoproteinemia
C0020541  |  portal hypertension
C0020532  |  hypersplenism
C0009324  |  ulcerative colitis
C0007134  |  renal cell carcinoma
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:11)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:16)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs386626619256982703717JAK2umls:C0856761BeFreeDiagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with Budd-Chiari syndrome and/or portal vein thrombosis.0.2557212222015NANANANANA
rs386626619167626263717JAK2umls:C0019154BeFreePrevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome.0.0035287442006NANANANANA
rs386626619256982703717JAK2umls:C0019154BeFreeDiagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with Budd-Chiari syndrome and/or portal vein thrombosis.0.0035287442015NANANANANA
rs386626619193086563717JAK2umls:C0019154BeFreeLow burden of a JAK2-V617F mutated clone in monoclonal haematopoiesis in a Japanese woman with Budd-Chiari syndrome.0.0035287442009NANANANANA
rs386626619193086563717JAK2umls:C0856761BeFreeLow burden of a JAK2-V617F mutated clone in monoclonal haematopoiesis in a Japanese woman with Budd-Chiari syndrome.0.2557212222009NANANANANA
rs386626619167626263717JAK2umls:C0856761BeFreePrevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome.0.2557212222006NANANANANA
rs386626619186001003717JAK2umls:C0019154BeFreeOccurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome.0.0035287442008NANANANANA
rs386626619186001003717JAK2umls:C0856761BeFreeOccurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome.0.2557212222008NANANANANA
rs77375493256982703717JAK2umls:C0019154BeFreeDiagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with Budd-Chiari syndrome and/or portal vein thrombosis.0.0035287442015JAK2;INSL695073770GA,T
rs77375493167626263717JAK2umls:C0856761BeFreePrevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome.0.2557212222006JAK2;INSL695073770GA,T
rs77375493186001003717JAK2umls:C0856761BeFreeOccurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome.0.2557212222008JAK2;INSL695073770GA,T
rs77375493256982703717JAK2umls:C0856761BeFreeDiagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with Budd-Chiari syndrome and/or portal vein thrombosis.0.2557212222015JAK2;INSL695073770GA,T
rs77375493193086563717JAK2umls:C0019154BeFreeLow burden of a JAK2-V617F mutated clone in monoclonal haematopoiesis in a Japanese woman with Budd-Chiari syndrome.0.0035287442009JAK2;INSL695073770GA,T
rs77375493167626263717JAK2umls:C0019154BeFreePrevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome.0.0035287442006JAK2;INSL695073770GA,T
rs77375493193086563717JAK2umls:C0856761BeFreeLow burden of a JAK2-V617F mutated clone in monoclonal haematopoiesis in a Japanese woman with Budd-Chiari syndrome.0.2557212222009JAK2;INSL695073770GA,T
rs77375493186001003717JAK2umls:C0019154BeFreeOccurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome.0.0035287442008JAK2;INSL695073770GA,T
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
C0019154amphetamineD000661300-62-9budd-chiari syndromeMESH:D006502marker/mechanism8583154
C0019154vinblastineD014747865-21-4budd-chiari syndromeMESH:D006502marker/mechanism509400
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)