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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: Dizziness (D004244)
Parent Node: Tremor (D014202)
..Starting node ..Primary orthostatic tremor (C536418)
Child Nodes:
Sister Nodes:
..Fragile X Tremor Ataxia Syndrome (C564105)
..Geniospasm (C537682)
..MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT (OMIM:300354)
..Primary orthostatic tremor (C536418)
..Tremor hereditary essential, 2 (C536546)
..Tremor of Intention, Ataxia, and Lipofuscinosis (C566038)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9288
Name:	Primary orthostatic tremor
Definition:
Alternative IDs:
ParentIDs:	MESH:D004244\|MESH:D014202
TreeNumbers:	C10.597.350.850/C536418 \|C10.597.751.237/C536418 \|C23.888.592.350.850/C536418 \|C23.888.592.763.237/C536418
Synonyms:	Orthostatic tremor, primary \|Shaky leg syndrome
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: C536418 MeSH: C536418 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants