MCID: KCN001

Kcna5-Related Familial Atrial Fibrillation malady

Genetic diseases, Rare diseases categories

Aliases & Classifications for Kcna5-Related Familial Atrial Fibrillation

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Aliases & Descriptions for Kcna5-Related Familial Atrial Fibrillation:

Name: Kcna5-Related Familial Atrial Fibrillation 20


Classifications:



Summaries for Kcna5-Related Familial Atrial Fibrillation

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MalaCards based summary: Kcna5-Related Familial Atrial Fibrillation An important gene associated with Kcna5-Related Familial Atrial Fibrillation is KCNA5 (potassium voltage-gated channel, shaker-related subfamily, member 5).

Symptoms for Kcna5-Related Familial Atrial Fibrillation

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Drugs & Therapeutics for Kcna5-Related Familial Atrial Fibrillation

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Drug clinical trials:

Search ClinicalTrials for Kcna5-Related Familial Atrial Fibrillation

Search NIH Clinical Center for Kcna5-Related Familial Atrial Fibrillation

Genetic Tests for Kcna5-Related Familial Atrial Fibrillation

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Genetic tests related to Kcna5-Related Familial Atrial Fibrillation:

id Genetic test Affiliating Genes
1 Kcna5-Related Familial Atrial Fibrillation20 KCNA5

Anatomical Context for Kcna5-Related Familial Atrial Fibrillation

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Animal Models for Kcna5-Related Familial Atrial Fibrillation or affiliated genes

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Publications for Kcna5-Related Familial Atrial Fibrillation

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Variations for Kcna5-Related Familial Atrial Fibrillation

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Expression for genes affiliated with Kcna5-Related Familial Atrial Fibrillation

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Search GEO for disease gene expression data for Kcna5-Related Familial Atrial Fibrillation.

Pathways for genes affiliated with Kcna5-Related Familial Atrial Fibrillation

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Compounds for genes affiliated with Kcna5-Related Familial Atrial Fibrillation

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GO Terms for genes affiliated with Kcna5-Related Familial Atrial Fibrillation

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Sources for Kcna5-Related Familial Atrial Fibrillation

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2CDC
12ExPASy
13FDA
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
33MeSH
34MESH via Orphanet
35MGI
38NCI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
57SNOMED-CT via Orphanet
61UMLS
62UMLS via Orphanet