Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Vertigo (D014717)
..Starting node ..Vertigo, Benign Recurrent, 2 (C567749)
Child Nodes:
Sister Nodes:
..Benign Paroxysmal Positional Vertigo (D065635)
..Episodic Ataxia, Type 3 (C564697)
..Vertigo, Benign Recurrent (C562859)
..Vertigo, Benign Recurrent, 1 (C567620)
..Vertigo, Benign Recurrent, 2 (C567749)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11591
Name:	Vertigo, Benign Recurrent, 2
Definition:
Alternative IDs:	OMIM:613106
ParentIDs:	MESH:D014717
TreeNumbers:	C09.218.568.900.883/C567749 \|C10.597.951/C567749 \|C23.888.592.958/C567749
Synonyms:	BRV2
Slim Mappings:	Ear-nose-throat disease\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: C567749 MeSH: C567749 OMIM: 613106; Genes:
Phenotypes
Disease Causing ClinVar Variants