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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: Brain Diseases (D001927)
Parent Node: Central Nervous System Infections (D002494)
Parent Node: Central Nervous System Viral Diseases (D020805)
..Starting node ..Encephalitis (D004660)
Child Nodes:
........Anti-N-Methyl-D-Aspartate Receptor Encephalitis (D060426)
........Cerebral Ventriculitis (D058565)
........Encephalitis, Viral (D018792) 16
........Encephalomyelitis (D004679) 8
........External Auditory Canal, Bilateral Atresia Of, With Congenital Vertical Talus (C566245)
........Leukoencephalitis, Acute Hemorrhagic (D004684) 1
........Limbic Encephalitis (D020363) 1
........Meningoencephalitis (D008590) 2
........Rasmussen Johnsen Thomsen syndrome (C535290)
........Rasmussen subacute encephalitis (C535291)
Sister Nodes:
..Encephalitis (D004660) 32
..Meningitis, Viral (D008587) 2
..Myelitis (D009187) 6
..Poliomyelitis (D011051) 2
..Pseudorabies (D011557)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3718
Name:	Encephalitis
Definition:	Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition.
Alternative IDs:
ParentIDs:	MESH:D001927\|MESH:D002494\|MESH:D020805
TreeNumbers:	C02.182.500 \|C10.228.140.430 \|C10.228.228.210.150 \|C10.228.228.245
Synonyms:	Brain Inflammation \|Brain Inflammations \|Encephalitides, Infectious \|Encephalitis, Infectious \|Encephalitis, Rasmussen \|Infectious Encephalitides \|Infectious Encephalitis \|Inflammation, Brain \|Rasmussen Encephalitis \|Rasmussen's Syndrome \|Rasmussen Syndrome
Slim Mappings:	Nervous system disease\|Viral disease
Reference:	MedGen: D004660 MeSH: D004660 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants