Disease browser and phenotype portal

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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: Gastrointestinal Neoplasms (D005770)
Parent Node: Intestinal Diseases (D007410)
Parent Node: Paraneoplastic Endocrine Syndromes (D009384)
Parent Node: Peptic Ulcer (D010437)
Parent Node: Stomach Diseases (D013272)
..Starting node ..Zollinger-Ellison Syndrome (D015043)
Child Nodes:
Sister Nodes:
..Achlorhydria (D000126)
..Diverticulosis, Stomach (D045724)
..Duodenogastric Reflux (D004383) 1
..Gastric Antral Vascular Ectasia (D020252) 1
..Gastric Dilatation (D013271)
..Gastric Outlet Obstruction (D017219) 8
..Gastritis (D005756) 3
..Gastroparesis (D018589)
..Peptic Ulcer (D010437) 9
..Postgastrectomy Syndromes (D011178) 1
..Stomach Neoplasms (D013274) 5
..Stomach Rupture (D013275)
..Stomach Volvulus (D013277) 1
..Zollinger-Ellison Syndrome (D015043)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11877
Name:	Zollinger-Ellison Syndrome
Definition:	A syndrome that is characterized by the triad of severe PEPTIC ULCER, hypersecretion of GASTRIC ACID, and GASTRIN-producing tumors of the PANCREAS or other tissue (GASTRINOMA). This syndrome may be sporadic or be associated with MULTIPLE ENDOCRINE NEOPLASIA TYPE 1.
Alternative IDs:
ParentIDs:	MESH:D005770\|MESH:D007410\|MESH:D009384\|MESH:D010437\|MESH:D013272
TreeNumbers:	C04.730.713.988 \|C06.301.371.883 \|C06.405.249.883 \|C06.405.469.965 \|C06.405.608.924 \|C06.405.748.947
Synonyms:	Syndrome, Zollinger-Ellison \|Zollinger Ellison Syndrome
Slim Mappings:	Cancer\|Digestive system disease
Reference:	MedGen: D015043 MeSH: D015043 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants