Zollinger-Ellison syndrome

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Information
Disease name
Zollinger-Ellison syndrome
Disease ID
DOID:0050782
Description
"A syndrome that is characterized by the development of a one or more tumors (gastrinoma) in the pancreas, duodenum, or both that secrete excessive levels of gastrin, a hormone that stimulates production of acid by the stomach." [url:http\://en.wikipedia.org/wiki/Zollinger-Ellison_Syndrome, url:http\://www.rarediseases.org/rare-disease-information/rare-diseases/byID/360/viewAbstract, url:https\://www.ncbi.nlm.nih.gov/pubmed/28949124, url:https\://www.niddk.nih.gov/health-information/digestive-diseases/zollinger-ellison-syndrome]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT00079833 Completed Phase 3 Esomeprazole In Patients With Gastric Acid Hypersecretory States Including Idiopathic Hypersecretion and Zollinger-Ellison Syndrome November 2003 July 2005
NCT00204373 Completed Phase 4 Treatment of Zollinger-Ellison Syndrome With Prevacid March 2003 December 2010
NCT02153398 Completed Phase 3 A Phase I/III Study of D961H 10 mg and 20 mg in Japanese Paediatric Patients With Gastrointestinal Acid Related Diseases June 2014 April 2016
NCT02454075 Terminated Phase 2 YF476 and Type II Gastric Carcinoids April 11, 2011 June 22, 2012
Disase is a (Disease Ontology)
DOID:225
Cross Reference ID (Disease Ontology)
GARD:7918
Cross Reference ID (Disease Ontology)
ICD10CM:E16.4
Cross Reference ID (Disease Ontology)
MESH:D015043
Cross Reference ID (Disease Ontology)
NCI:C3453
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:267477002
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0043515
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0002044
OrphaNumber from OrphaNet (Orphanet)
913
MeSH unique ID (MeSH (Medical Subject Headings))
D015043