MCID: GBR004
MIFTS: 6

Gabrg2-Related Dravet Syndrome malady

Categories: Genetic diseases, Rare diseases, Neuronal diseases

Aliases & Classifications for Gabrg2-Related Dravet Syndrome

Aliases & Descriptions for Gabrg2-Related Dravet Syndrome:

Name: Gabrg2-Related Dravet Syndrome 24
Gabrg2-Related Severe Myoclonic Epilepsy of Infancy 24

Classifications:



Summaries for Gabrg2-Related Dravet Syndrome

MalaCards based summary : Gabrg2-Related Dravet Syndrome, is also known as gabrg2-related severe myoclonic epilepsy of infancy. An important gene associated with Gabrg2-Related Dravet Syndrome is GABRG2 (Gamma-Aminobutyric Acid Type A Receptor Gamma2 Subunit).

Related Diseases for Gabrg2-Related Dravet Syndrome

Diseases in the Dravet Syndrome family:

Gabrg2-Related Dravet Syndrome Scn9a-Related Dravet Syndrome

Symptoms & Phenotypes for Gabrg2-Related Dravet Syndrome

Drugs & Therapeutics for Gabrg2-Related Dravet Syndrome

Search Clinical Trials , NIH Clinical Center for Gabrg2-Related Dravet Syndrome

Genetic Tests for Gabrg2-Related Dravet Syndrome

Genetic tests related to Gabrg2-Related Dravet Syndrome:

id Genetic test Affiliating Genes
1 Gabrg2-Related Dravet Syndrome 24 GABRG2

Anatomical Context for Gabrg2-Related Dravet Syndrome

Publications for Gabrg2-Related Dravet Syndrome

Variations for Gabrg2-Related Dravet Syndrome

Expression for Gabrg2-Related Dravet Syndrome

Search GEO for disease gene expression data for Gabrg2-Related Dravet Syndrome.

Pathways for Gabrg2-Related Dravet Syndrome

GO Terms for Gabrg2-Related Dravet Syndrome

Sources for Gabrg2-Related Dravet Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 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 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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