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: Pancreatic Diseases (D010182)
..Starting node ..Exocrine Pancreatic Insufficiency (D010188)
Child Nodes:
........Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis (C567195)
........Pancreatic Insufficiency, Combined Exocrine (C564907)
........Shwachman syndrome (C537330)
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:	4021
Name:	Exocrine Pancreatic Insufficiency
Definition:	A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE) by the EXOCRINE PANCREAS into the DUODENUM. This condition is often associated with CYSTIC FIBROSIS and with chronic PANCREATITIS.
Alternative IDs:
ParentIDs:	MESH:D010182
TreeNumbers:	C06.689.276
Synonyms:	Exocrine Pancreatic Insufficiencies \|Insufficiencies, Exocrine Pancreatic \|Insufficiencies, Pancreatic \|Insufficiency, Exocrine Pancreatic \|Insufficiency, Pancreatic \|Pancreatic Insufficiencies \|Pancreatic Insufficiencies, Exocrine \|Pancreatic Insufficiency \|Pan
Slim Mappings:	Digestive system disease
Reference:	MedGen: D010188 MeSH: D010188 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants