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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: Postoperative Complications (D011183)
Parent Node: Stomach Diseases (D013272)
..Starting node ..Postgastrectomy Syndromes (D011178)
Child Nodes:
........Dumping Syndrome (D004377)
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:	9170
Name:	Postgastrectomy Syndromes
Definition:	Sequelae of gastrectomy from the second week after operation on. Include recurrent or anastomotic ulcer, postprandial syndromes (DUMPING SYNDROME and late postprandial hypoglycemia), disordered bowel action, and nutritional deficiencies.
Alternative IDs:
ParentIDs:	MESH:D011183\|MESH:D013272
TreeNumbers:	C06.405.748.630 \|C23.550.767.812
Synonyms:	Postgastrectomy Syndrome \|Syndrome, Postgastrectomy \|Syndromes, Postgastrectomy
Slim Mappings:	Digestive system disease\|Pathology (process)
Reference:	MedGen: D011178 MeSH: D011178 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants