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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: Movement Disorders (D009069)
..Starting node ..Essential Tremor (D020329)
Child Nodes:
........Tremor hereditary essential, 1 (C536545)
........Tremor, Hereditary Essential, 3 (C566949)
........Tremor, Hereditary Essential, And Idiopathic Normal Pressure Hydrocephalus (C567519)
Sister Nodes:
..Akathisia, Drug-Induced (D017109)
..Angelman Syndrome (D017204) 1
..Beta-Ureidopropionase Deficiency (C563210)
..Dyskinesias (D020820) 199
..Dystonic Disorders (D020821) 31
..Essential Tremor (D020329) 3
..Guanidinoacetate methyltransferase deficiency (C537622)
..Hepatolenticular Degeneration (D006527) 2
..Multiple System Atrophy (D019578) 21
..Non-lissencephalic cortical dysplasia (C536243)
..Pantothenate Kinase-Associated Neurodegeneration (D006211) 1
..Parkinsonian Disorders (D020734) 39
..Paroxysmal Tonic Upgaze, Benign Childhood, With Ataxia (C566817)
..Pronation-Supination Of The Forearm, Impairment Of (C566757)
..Supranuclear Palsy, Progressive (D013494) 5
..Telfer Sugar Jaeger syndrome (C536955)
..Tic Disorders (D013981) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4001
Name:	Essential Tremor
Definition:	A relatively common disorder characterized by a fairly specific pattern of tremors which are most prominent in the upper extremities and neck, inducing titubations of the head. The tremor is usually mild, but when severe may be disabling. An autosomal dominant pattern of inheritance may occur in some families (i.e., familial tremor). (Mov Disord 1988;13(1):5-10)
Alternative IDs:
ParentIDs:	MESH:D009069
TreeNumbers:	C10.228.662.350
Synonyms:	Benign Essential Tremor \|Benign Essential Tremors \|Essential Tremor, Benign \|Essential Tremors \|Essential Tremors, Benign \|Familial Tremor \|Familial Tremors \|Hereditary Essential Tremor \|Tremor, Benign Essential \|Tremor, Essential \|Tremor, Familial \|Tremors, Benign
Slim Mappings:	Nervous system disease
Reference:	MedGen: D020329 MeSH: D020329 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants