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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 Diseases (D010182)
..Starting node ..Pancreatitis (D010195)
Child Nodes:
........Pancreatitis, Acute Necrotizing (D019283)
........Pancreatitis, Alcoholic (D019512)
........Pancreatitis, Chronic (D050500) 4
........Pancreatitis, Graft (D055589)
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:	8553
Name:	Pancreatitis
Definition:	INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis.
Alternative IDs:
ParentIDs:	MESH:D010182
TreeNumbers:	C06.689.750
Synonyms:	Pancreatitides
Slim Mappings:	Digestive system disease
Reference:	MedGen: D010195 MeSH: D010195 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants