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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: Encephalitis (D004660)
Parent Node: Inflammation (D007249)
..Starting node ..Rasmussen subacute encephalitis (C535291)
Child Nodes:
Sister Nodes:
..Acute-Phase Reaction (D000210)
..Foreign-Body Reaction (D005549) 2
..Neurogenic Inflammation (D020078)
..Rasmussen subacute encephalitis (C535291)
..Seroma (D049291)
..Serositis (D012700)
..Suppuration (D013492) 31
..Systemic Inflammatory Response Syndrome (D018746) 11
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9603
Name:	Rasmussen subacute encephalitis
Definition:
Alternative IDs:
ParentIDs:	MESH:D004660\|MESH:D007249
TreeNumbers:	C02.182.500/C535291 \|C10.228.140.430/C535291 \|C10.228.228.210.150/C535291 \|C10.228.228.245/C535291 \|C23.550.470/C535291
Synonyms:	Subacute focal encephalitis of Rasmussen
Slim Mappings:	Nervous system disease\|Pathology (process)\|Viral disease
Reference:	MedGen: C535291 MeSH: C535291 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants