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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: Orthostatic Intolerance (D054971)
..Starting node ..Postural Orthostatic Tachycardia Syndrome (D054972)
Child Nodes:
Sister Nodes:
..Hypotension, Orthostatic (D007024) 2
..Irritable heart (C531763)
..Post-Exercise Hypotension (D057774)
..Postural Orthostatic Tachycardia Syndrome (D054972)
..Syncope, Vasovagal (D019462) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9183
Name:	Postural Orthostatic Tachycardia Syndrome
Definition:	A syndrome of ORTHOSTATIC INTOLERANCE combined with excessive upright TACHYCARDIA, and usually without associated ORTHOSTATIC HYPOTENSION. All variants have in common an excessively reduced venous return to the heart (central HYPOVOLEMIA) while upright.
Alternative IDs:
ParentIDs:	MESH:D054971
TreeNumbers:	C10.177.575.600.625
Synonyms:	Postural Tachycardia Syndrome \|Syndrome, Postural Tachycardia \|Tachycardia Syndrome, Postural
Slim Mappings:	Nervous system disease
Reference:	MedGen: D054972 MeSH: D054972 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants