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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: Pancreatic Diseases (D010182)
..Starting node ..Pancreatic Cyst (D010181)
Child Nodes:
........Pancreatic Pseudocyst (D010192)
........Renal hepatic pancreatic dysplasia Dandy Walker cyst (C537756)
Sister Nodes:
..Annular pancreas (C536376)
..Congenital Hyperinsulinism (D044903) 2
..Cystic Fibrosis (D003550) 4
..Exocrine Pancreatic Insufficiency (D010188) 3
..Johanson Blizzard syndrome (C535880)
..Pancreatic Agenesis, Congenital (C564908)
..Pancreatic Cyst (D010181) 2
..Pancreatic Fistula (D010185)
..Pancreatic lipomatosis duodenal stenosis (C535839)
..Pancreatic Neoplasms (D010190) 20
..Pancreatitis (D010195) 8
..RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8543
Name:	Pancreatic Cyst
Definition:	A true cyst of the PANCREAS, distinguished from the much more common PANCREATIC PSEUDOCYST by possessing a lining of mucous EPITHELIUM. Pancreatic cysts are categorized as congenital, retention, neoplastic, parasitic, enterogenous, or dermoid. Congenital cysts occur more frequently as solitary cysts but may be multiple. Retention cysts are gross enlargements of PANCREATIC DUCTS secondary to ductal obstruction. (From Bockus Gastroenterology, 4th ed, p4145)
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D010182
TreeNumbers:	C04.182.640 \|C06.689.500
Synonyms:	Cyst, Pancreatic \|Cysts, Pancreatic \|Pancreatic Cysts
Slim Mappings:	Cancer\|Digestive system disease
Reference:	MedGen: D010181 MeSH: D010181 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants