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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: Mediastinitis (D008480)
Parent Node: Sclerosis (D012598)
..Starting node ..Mediastinal Fibrosis (C536136)
Child Nodes:
Sister Nodes:
..Mediastinal Fibrosis (C536136)
..Mesangial sclerosis, diffuse (C537346)
..Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities (C565405)
..Osteosclerosis with ichthyosis and premature ovarian failure (C536064)
..Poikiloderma, Hereditary Sclerosing (C562824)
..Scleroatonic muscular dystrophy (C537521)
..Sclerosing bone dysplasia mental retardation (C537523)
..Sclerosing lymphocytic lobulitis (C537524)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6876
Name:	Mediastinal Fibrosis
Definition:
Alternative IDs:
ParentIDs:	MESH:D008480\|MESH:D012598
TreeNumbers:	C08.846.187.790/C536136 \|C23.550.823/C536136
Synonyms:	Fibrosing mediastinitis \|Idiopathic mediastinal fibrosis \|Sclerosing mediastinitis
Slim Mappings:	Pathology (process)\|Respiratory tract disease
Reference:	MedGen: C536136 MeSH: C536136 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants