Disease browser and phenotype portal

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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: Sensation Disorders (D012678)
..Starting node ..Dizziness (D004244)
Child Nodes:
........Primary orthostatic tremor (C536418)
Sister Nodes:
..Dizziness (D004244) 1
..Hearing Disorders (D006311) 403
..Olfaction Disorders (D000857) 4
..Posterior column ataxia (C536342)
..Somatosensory Disorders (D020886) 6
..Taste Disorders (D013651) 3
..Vision Disorders (D014786) 84
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3433
Name:	Dizziness
Definition:	An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness.
Alternative IDs:
ParentIDs:	MESH:D012678
TreeNumbers:	C10.597.751.237 \|C23.888.592.763.237
Synonyms:	Dizzyness \|Lightheadedness \|Light Headedness \|Light-Headedness \|Orthostasis
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D004244 MeSH: D004244 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants