MCID: VRT008
MIFTS: 7

Vertigo, Benign Recurrent, 2

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 73
Brv2 57

Classifications:



External Ids:

OMIM 57 613106
UMLS 73 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).

Description 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 11.1

Symptoms & Phenotypes for Vertigo, Benign Recurrent, 2

Clinical features from OMIM:

613106

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

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 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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