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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: Malabsorption Syndromes (D008286)
Parent Node: Postoperative Complications (D011183)
..Starting node ..Short Bowel Syndrome (D012778)
Child Nodes:
Sister Nodes:
..Afferent Loop Syndrome (D000343)
..Anastomotic Leak (D057868)
..Corneal Endothelial Cell Loss (D055954)
..Coronary-Subclavian Steal Syndrome (D058686)
..Delayed Emergence from Anesthesia (D055191)
..Failed Back Surgery Syndrome (D055111)
..Gas bloat syndrome (C535647)
..Graft Occlusion, Vascular (D006083)
..Malignant Hyperthermia (D008305) 12
..Pain, Postoperative (D010149) 1
..Postcholecystectomy Syndrome (D017562)
..Postgastrectomy Syndromes (D011178) 1
..Postoperative Hemorrhage (D019106) 1
..Postoperative Nausea and Vomiting (D020250)
..Postpericardiotomy Syndrome (D011185)
..Prosthesis Failure (D011475) 1
..Prosthesis-Related Infections (D016459)
..Reperfusion Injury (D015427) 2
..Shock, Surgical (D012773)
..Short Bowel Syndrome (D012778)
..Slit Ventricle Syndrome (D056124)
..Surgical Wound Dehiscence (D013529)
..Surgical Wound Infection (D013530)
..Vasoplegia (D056987)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10185
Name:	Short Bowel Syndrome
Definition:	A malabsorption syndrome resulting from extensive operative resection of the SMALL INTESTINE, the absorptive region of the GASTROINTESTINAL TRACT.
Alternative IDs:
ParentIDs:	MESH:D008286\|MESH:D011183
TreeNumbers:	C06.405.469.637.832 \|C23.550.767.882
Synonyms:	Bowel Syndrome, Short \|Bowel Syndromes, Short \|Short Bowel Syndromes \|Syndrome, Short Bowel \|Syndromes, Short Bowel
Slim Mappings:	Digestive system disease\|Pathology (process)
Reference:	MedGen: D012778 MeSH: D012778 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants