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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: Central Nervous System Diseases (D002493)
Parent Node: Central Nervous System Infections (D002494)
Parent Node: Encephalitis (D004660)
..Starting node ..Encephalomyelitis (D004679)
Child Nodes:
........Encephalomyelitis, Equine (D004683) 3
........Fatigue Syndrome, Chronic (D015673)
........Leukoencephalitis, Acute Hemorrhagic (D004684) 1
........Progressive Encephalomyelitis with Rigidity (C566113)
Sister 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)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3734
Name:	Encephalomyelitis
Definition:	A general term indicating inflammation of the BRAIN and SPINAL CORD, often used to indicate an infectious process, but also applicable to a variety of autoimmune and toxic-metabolic conditions. There is significant overlap regarding the usage of this term and ENCEPHALITIS in the literature.
Alternative IDs:
ParentIDs:	MESH:D002493\|MESH:D002494\|MESH:D004660
TreeNumbers:	C10.228.140.430.500 \|C10.228.228.291 \|C10.228.440
Synonyms:	Encephalomyelitis, Inflammatory \|Inflammatory Encephalomyelitis \|Myeloencephalitides \|Myeloencephalitis
Slim Mappings:	Nervous system disease
Reference:	MedGen: D004679 MeSH: D004679 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants