MCID: GBR004

Gabrg2-Related Dravet Syndrome malady

Categories: Genetic diseases, Rare diseases, Neuronal diseases

Aliases & Classifications for Gabrg2-Related Dravet Syndrome

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Aliases & Descriptions for Gabrg2-Related Dravet Syndrome:

Name: Gabrg2-Related Dravet Syndrome 22
 
Gabrg2-Related Severe Myoclonic Epilepsy of Infancy 22

Classifications:



Summaries for Gabrg2-Related Dravet Syndrome

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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

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Diseases in the Dravet Syndrome family:

gabrg2-related dravet syndrome Scn9a-Related Dravet Syndrome

Symptoms for Gabrg2-Related Dravet Syndrome

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Drugs & Therapeutics for Gabrg2-Related Dravet Syndrome

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Interventional clinical trials:

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

Genetic Tests for Gabrg2-Related Dravet Syndrome

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Genetic tests related to Gabrg2-Related Dravet Syndrome:

id Genetic test Affiliating Genes
1 Gabrg2-Related Dravet Syndrome22 GABRG2

Anatomical Context for Gabrg2-Related Dravet Syndrome

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Animal Models for Gabrg2-Related Dravet Syndrome or affiliated genes

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Publications for Gabrg2-Related Dravet Syndrome

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Variations for Gabrg2-Related Dravet Syndrome

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Expression for genes affiliated with Gabrg2-Related Dravet Syndrome

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

Pathways for genes affiliated with Gabrg2-Related Dravet Syndrome

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GO Terms for genes affiliated with Gabrg2-Related Dravet Syndrome

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Sources for Gabrg2-Related Dravet Syndrome

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2CDC
14ExPASy
15FDA
16FMA
24GTR
25HGMD
26HMDB
27ICD10
28ICD10 via Orphanet
29ICD9CM
30IUPHAR
31KEGG
34MedGen
36MeSH
37MESH via Orphanet
38MGI
41NCI
42NCIt
43NDF-RT
46NINDS
47Novoseek
49OMIM
50OMIM via Orphanet
54PubMed
55QIAGEN
60SNOMED-CT via Orphanet
64Tumor Gene Family of Databases
65UMLS
66UMLS via Orphanet