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: Paralysis (D010243)
Parent Node: Stomach Diseases (D013272)
..Starting node ..Gastroparesis (D018589)
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:	4530
Name:	Gastroparesis
Definition:	Chronic delayed gastric emptying. Gastroparesis may be caused by motor dysfunction or paralysis of STOMACH muscles or may be associated with other systemic diseases such as DIABETES MELLITUS.
Alternative IDs:
ParentIDs:	MESH:D010243\|MESH:D013272
TreeNumbers:	C06.405.748.543 \|C23.888.592.636.263
Synonyms:	Gastric Stases \|Gastric Stasis \|Gastropareses \|Stases, Gastric \|Stasis, Gastric
Slim Mappings:	Digestive system disease\|Signs and symptoms
Reference:	MedGen: D018589 MeSH: D018589 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants