Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandLiver Diseases (D008107)
Parent Node:
expandVenous Thrombosis (D020246)
..Starting node
..expandBudd-Chiari Syndrome (D006502)

       Child Nodes:
........expandMembranous Obstruction of Inferior Vena Cava (C563013)



 Sister Nodes: 
..expandBudd-Chiari Syndrome (D006502) Child1
..expandPostthrombotic Syndrome (D054070)
..expandRetinal Vein Occlusion (D012170)
..expandThrombophlebitis (D013924) Child1
..expandUpper Extremity Deep Vein Thrombosis (D056824)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1527
Name:Budd-Chiari Syndrome
Definition:A condition in which the hepatic venous outflow is obstructed anywhere from the small HEPATIC VEINS to the junction of the INFERIOR VENA CAVA and the RIGHT ATRIUM. Usually the blockage is extrahepatic and caused by blood clots (THROMBUS) or fibrous webs. Parenchymal FIBROSIS is uncommon.
Alternative IDs:OMIM:600880
ParentIDs:MESH:D008107|MESH:D020246
TreeNumbers:C06.552.347 |C14.907.355.830.925.275
Synonyms:BDCHS |Budd Chiari Syndrome |Chiari's Syndrome |Chiaris Syndrome |Chiari Syndrome |Hepatic Vein Thromboses |Hepatic Vein Thrombosis |Hepatic Venous Outflow Obstruction |MEMBRANOUS OBSTRUCTION OF INFERIOR VENA CAVA, INCLUDED |MOVC, INCLUDED |Thromboses, Hepatic Vei
Slim Mappings:Cardiovascular disease|Digestive system disease
Reference: MedGen: D006502
MeSH: D006502
OMIM: 600880;

Genes: JAK2;
Phenotypes
1 HP:0002639Budd-Chiari syndrome
2 HP:0001394Cirrhosis
3 HP:0001402Hepatocellular carcinoma
Disease Causing ClinVar Variants