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: Orthostatic Intolerance (D054971)
..Starting node ..Irritable heart (C531763)
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:	5919
Name:	Irritable heart
Definition:
Alternative IDs:
ParentIDs:	MESH:D054971
TreeNumbers:	C10.177.575.600/C531763 \|C23.888.592.610/C531763
Synonyms:	Soldiers heart
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: C531763 MeSH: C531763 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants