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: Cysts (D003560)
Parent Node: Peritoneal Neoplasms (D010534)
..Starting node ..Mesenteric Cyst (D008639)
Child Nodes:
Sister Nodes:
..Mesenteric Cyst (D008639)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7091
Name:	Mesenteric Cyst
Definition:	A rare intra-abdominal tumor in the MESENTERY. Mesenteric cysts are usually benign and can be very large fluid-filled (2000 mL) lesions.
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D010534
TreeNumbers:	C04.182.473 \|C06.844.620.500
Synonyms:	Cyst, Mesenteric \|Cysts, Mesenteric \|Mesenteric Cysts
Slim Mappings:	Cancer\|Digestive system disease
Reference:	MedGen: D008639 MeSH: D008639 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants