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: Cysts (D003560)
Parent Node: Esophageal Diseases (D004935)
..Starting node ..Esophageal Cyst (D004934)
Child Nodes:
Sister Nodes:
..Barrett Esophagus (D001471) 1
..Deglutition Disorders (D003680) 19
..Diverticulosis, Esophageal (D045723)
..Esophageal and Gastric Varices (D004932)
..Esophageal Atresia (D004933) 2
..Esophageal Cyst (D004934)
..Esophageal Fistula (D004937) 5
..Esophageal Neoplasms (D004938) 4
..Esophageal Perforation (D004939) 2
..Esophageal Stenosis (D004940)
..Esophagitis (D004941) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3988
Name:	Esophageal Cyst
Definition:	Any fluid-filled closed cavity or sac (CYSTS) that is lined by an EPITHELIUM and found in the ESOPHAGUS region.
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D004935
TreeNumbers:	C04.182.281 \|C06.405.117.316
Synonyms:	Cyst, Esophageal \|Cysts, Esophageal \|Esophageal Cysts
Slim Mappings:	Cancer\|Digestive system disease
Reference:	MedGen: D004934 MeSH: D004934 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants