BRV2
MCID: VRT008
MIFTS: 9

Vertigo, Benign Recurrent, 2 (BRV2)

Categories: Genetic diseases

Aliases & Classifications for Vertigo, Benign Recurrent, 2

MalaCards integrated aliases for Vertigo, Benign Recurrent, 2:

Name: Vertigo, Benign Recurrent, 2 57 13 70
Brv2 57

Classifications:



External Ids:

OMIM® 57 613106
UMLS 70 C2751289

Summaries for Vertigo, Benign Recurrent, 2

MalaCards based summary : Vertigo, Benign Recurrent, 2, also known as brv2, is related to vertigo, benign recurrent. An important gene associated with Vertigo, Benign Recurrent, 2 is BRV2 (Vertigo, Benign Recurrent, 2).

More information from OMIM: 613106

Related Diseases for Vertigo, Benign Recurrent, 2

Diseases in the Vertigo, Benign Recurrent family:

Vertigo, Benign Recurrent, 2

Diseases related to Vertigo, Benign Recurrent, 2 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 vertigo, benign recurrent 10.9

Symptoms & Phenotypes for Vertigo, Benign Recurrent, 2

Clinical features from OMIM®:

613106 (Updated 20-May-2021)

Drugs & Therapeutics for Vertigo, Benign Recurrent, 2

Search Clinical Trials , NIH Clinical Center for Vertigo, Benign Recurrent, 2

Genetic Tests for Vertigo, Benign Recurrent, 2

Anatomical Context for Vertigo, Benign Recurrent, 2

Publications for Vertigo, Benign Recurrent, 2

Articles related to Vertigo, Benign Recurrent, 2:

# Title Authors PMID Year
1
A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. 57
16330481 2006
2
Molecular and phylogenetic analyses of bovine rhinovirus type 2 shows it is closely related to foot-and-mouth disease virus. 61
18201745 2008

Variations for Vertigo, Benign Recurrent, 2

Expression for Vertigo, Benign Recurrent, 2

Search GEO for disease gene expression data for Vertigo, Benign Recurrent, 2.

Pathways for Vertigo, Benign Recurrent, 2

GO Terms for Vertigo, Benign Recurrent, 2

Sources for Vertigo, Benign Recurrent, 2

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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