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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: Torticollis (D014103)
..Starting node ..Cervical Dystonia, Primary (C566572)
Child Nodes:
Sister Nodes:
..Cervical Dystonia, Primary (C566572)
..Congenital torticollis (C535425)
..Contractures, Congenital, Torticollis, and Malignant Hyperthermia (C565679)
..Sandifer syndrome (C537234)
..Torticollis keloids cryptorchidism renal dysplasia (C536970)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1985
Name:	Cervical Dystonia, Primary
Definition:
Alternative IDs:
ParentIDs:	MESH:D014103
TreeNumbers:	C10.228.662.300.750/C566572 \|C10.597.350.300.800/C566572 \|C23.888.592.350.300.800/C566572
Synonyms:	Dystonia, Primary Cervical
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: C566572 MeSH: C566572 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants