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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: Sarcoidosis (D012507)
..Starting node ..Neurosarcoidosis (C535814)
Child Nodes:
Sister Nodes:
..Neurosarcoidosis (C535814)
..Sarcoidosis, Early-Onset (C563714)
..Sarcoidosis, Pulmonary (D017565)
..Uveoparotid Fever (D014608)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8010
Name:	Neurosarcoidosis
Definition:
Alternative IDs:
ParentIDs:	MESH:D002493\|MESH:D012507
TreeNumbers:	C10.228/C535814 \|C15.604.515.827/C535814
Synonyms:	Nervous system sarcoidosis
Slim Mappings:	Lymphatic disease\|Nervous system disease
Reference:	MedGen: C535814 MeSH: C535814 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants