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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: Mediastinal Diseases (D008477)
..Starting node ..Mediastinal Cyst (D008476)
Child Nodes:
Sister Nodes:
..Boerhaave syndrome (C536571)
..Mediastinal Cyst (D008476)
..Mediastinal Emphysema (D008478)
..Mediastinal Neoplasms (D008479)
..Mediastinitis (D008480) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6873
Name:	Mediastinal Cyst
Definition:	Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus.
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D008477
TreeNumbers:	C04.182.444 \|C08.846.187.145
Synonyms:	Cyst, Mediastinal \|Cyst, Pericardial \|Cysts, Mediastinal \|Cysts, Pericardial \|Cysts, Thoracic \|Cysts, Thymic \|Cysts, Tracheal \|Cyst, Thoracic \|Cyst, Thymic \|Cyst, Tracheal \|Mediastinal Cysts \|Pericardial Cyst \|Pericardial Cysts \|Thoracic Cyst \|Thoracic Cysts \|Thymic Cy
Slim Mappings:	Cancer\|Respiratory tract disease
Reference:	MedGen: D008476 MeSH: D008476 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants