Disease browser and phenotype portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Arterial Occlusive Diseases (D001157)
Parent Node: Intestinal Diseases (D007410)
Parent Node: Peritoneal Diseases (D010532)
..Starting node ..Mesenteric Vascular Occlusion (D008641)
Child Nodes:
Sister Nodes:
..Chylous Ascites (D002915) 1
..Hemoperitoneum (D006465)
..Mesenteric Ischemia (D065666)
..Mesenteric Lymphadenitis (D008640)
..Mesenteric Vascular Occlusion (D008641)
..Panniculitis, Peritoneal (D015436) 1
..Peritoneal Fibrosis (D056627)
..Peritoneal Neoplasms (D010534) 1
..Peritonitis (D010538) 3
..Pneumoperitoneum (D011027)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7094
Name:	Mesenteric Vascular Occlusion
Definition:	Obstruction of the flow in the SPLANCHNIC CIRCULATION by ATHEROSCLEROSIS; EMBOLISM; THROMBOSIS; STENOSIS; TRAUMA; and compression or intrinsic pressure from adjacent tumors. Rare causes are drugs, intestinal parasites, and vascular immunoinflammatory diseases such as PERIARTERITIS NODOSA and THROMBOANGIITIS OBLITERANS. (From Juergens et al., Peripheral Vascular Diseases, 5th ed, pp295-6)
Alternative IDs:
ParentIDs:	MESH:D001157\|MESH:D007410\|MESH:D010532
TreeNumbers:	C06.405.469.675 \|C06.844.550 \|C14.907.137.534
Synonyms:	Mesenteric Vascular Occlusions \|Occlusion, Mesenteric Vascular \|Occlusions, Mesenteric Vascular \|Vascular Occlusion, Mesenteric \|Vascular Occlusions, Mesenteric
Slim Mappings:	Cardiovascular disease\|Digestive system disease
Reference:	MedGen: D008641 MeSH: D008641 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants