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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: Pancreatic Cyst (D010181)
..Starting node ..Pancreatic Pseudocyst (D010192)
Child Nodes:
Sister Nodes:
..Pancreatic Pseudocyst (D010192)
..Renal hepatic pancreatic dysplasia Dandy Walker cyst (C537756)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8552
Name:	Pancreatic Pseudocyst
Definition:	Cyst-like space not lined by EPITHELIUM and contained within the PANCREAS. Pancreatic pseudocysts account for most of the cystic collections in the pancreas and are often associated with chronic PANCREATITIS.
Alternative IDs:
ParentIDs:	MESH:D010181
TreeNumbers:	C04.182.640.692 \|C06.689.500.692
Synonyms:	Pancreatic Pseudocysts \|Pseudocyst, Pancreatic \|Pseudocysts, Pancreatic
Slim Mappings:	Cancer\|Digestive system disease
Reference:	MedGen: D010192 MeSH: D010192 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants