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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: Mediastinal Diseases (D008477)
..Starting node ..Mediastinitis (D008480)
Child Nodes:
........Mediastinal Fibrosis (C536136)
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:	6878
Name:	Mediastinitis
Definition:	Inflammation of the mediastinum, the area between the pleural sacs.
Alternative IDs:
ParentIDs:	MESH:D008477
TreeNumbers:	C08.846.187.790
Synonyms:	Inflammation, Mediastinum \|Inflammations, Mediastinum \|Mediastinitides \|Mediastinum Inflammation \|Mediastinum Inflammations
Slim Mappings:	Respiratory tract disease
Reference:	MedGen: D008480 MeSH: D008480 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants