Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Digestive System Diseases (D004066)
..Starting node ..Pancreatic Diseases (D010182)
Child 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)
Sister Nodes:
..Biliary Tract Diseases (D001660) 68
..Digestive System Abnormalities (D004065) 78
..Digestive System Fistula (D016154) 12
..Digestive System Neoplasms (D004067) 99
..Gastrointestinal Diseases (D005767) 357
..Liver Diseases (D008107) 135
..Novak syndrome (C537851)
..Pancreatic Diseases (D010182) 51
..Peritoneal Diseases (D010532) 16
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8544
Name:	Pancreatic Diseases
Definition:	Pathological processes of the PANCREAS.
Alternative IDs:
ParentIDs:	MESH:D004066
TreeNumbers:	C06.689
Synonyms:	Disease, Pancreatic \|Diseases, Pancreatic \|Pancreatic Disease
Slim Mappings:	Digestive system disease
Reference:	MedGen: D010182 MeSH: D010182 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants