MCID: NXN002

Nexn-Related Familial Hypertrophic Cardiomyopathy malady

Categories: Genetic diseases, Cardiovascular diseases, Rare diseases, Metabolic diseases

Aliases & Classifications for Nexn-Related Familial Hypertrophic Cardiomyopathy

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Aliases & Descriptions for Nexn-Related Familial Hypertrophic Cardiomyopathy:

Name: Nexn-Related Familial Hypertrophic Cardiomyopathy 22

Classifications:



Summaries for Nexn-Related Familial Hypertrophic Cardiomyopathy

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MalaCards based summary: Nexn-Related Familial Hypertrophic Cardiomyopathy An important gene associated with Nexn-Related Familial Hypertrophic Cardiomyopathy is NEXN (Nexilin F-Actin Binding Protein).

Related Diseases for Nexn-Related Familial Hypertrophic Cardiomyopathy

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Diseases in the Hypertrophic Cardiomyopathy family:

Cardiomyopathy, Hypertrophic, 20 Cardiomyopathy, Hypertrophic, 2
Cardiomyopathy, Familial Hypertrophic, 9 Cardiomyopathy, Familial Hypertrophic
Cardiomyopathy, Hypertrophic, 13 Cardiomyopathy, Hypertrophic, 8
Cardiomyopathy, Hypertrophic, 16 Cardiomyopathy, Hypertrophic, 18
Cardiomyopathy, Hypertrophic 6 Cardiomyopathy, Hypertrophic, 15
Cardiomyopathy, Hypertrophic, 12 Cardiomyopathy, Hypertrophic, 4
Cardiomyopathy, Hypertrophic, 10 Cardiomyopathy, Hypertrophic, 14
Cardiomyopathy, Hypertrophic, 11 Cardiomyopathy, Hypertrophic, 3
Cardiomyopathy, Hypertrophic, 25 Cardiomyopathy, Hypertrophic, 19
Cardiomyopathy, Hypertrophic, 7 Cardiomyopathy, Hypertrophic, 17
Calr3-Related Familial Hypertrophic Cardiomyopathy Jph2-Related Familial Hypertrophic Cardiomyopathy
Actc1-Related Familial Hypertrophic Cardiomyopathy Actn2-Related Familial Hypertrophic Cardiomyopathy
Cav3-Related Hypertrophic Cardiomyopathy Csrp3-Related Familial Hypertrophic Cardiomyopathy
Mybpc3-Related Familial Hypertrophic Cardiomyopathy Myh6-Related Familial Hypertrophic Cardiomyopathy
Myh7-Related Familial Hypertrophic Cardiomyopathy Myl2-Related Familial Hypertrophic Cardiomyopathy
Myl3-Related Familial Hypertrophic Cardiomyopathy Myoz2-Related Familial Hypertrophic Cardiomyopathy
nexn-related familial hypertrophic cardiomyopathy Pln-Related Familial Hypertrophic Cardiomyopathy
Tcap-Related Familial Hypertrophic Cardiomyopathy Tnnc1-Related Familial Hypertrophic Cardiomyopathy
Tnni3-Related Familial Hypertrophic Cardiomyopathy Tnnt2-Related Familial Hypertrophic Cardiomyopathy
Tpm1-Related Familial Hypertrophic Cardiomyopathy Ttn-Related Familial Hypertrophic Cardiomyopathy
Vcl-Related Familial Hypertrophic Cardiomyopathy Hypertrophic Cardiomyopathy Due to Intensive Athletic Training
Fatal Congenital Hypertrophic Cardiomyopathy Due to Glycogen Storage Disease

Symptoms for Nexn-Related Familial Hypertrophic Cardiomyopathy

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Drugs & Therapeutics for Nexn-Related Familial Hypertrophic Cardiomyopathy

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Nexn-Related Familial Hypertrophic Cardiomyopathy

Genetic Tests for Nexn-Related Familial Hypertrophic Cardiomyopathy

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Genetic tests related to Nexn-Related Familial Hypertrophic Cardiomyopathy:

id Genetic test Affiliating Genes
1 Nexn-Related Familial Hypertrophic Cardiomyopathy22 NEXN

Anatomical Context for Nexn-Related Familial Hypertrophic Cardiomyopathy

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Animal Models for Nexn-Related Familial Hypertrophic Cardiomyopathy or affiliated genes

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Publications for Nexn-Related Familial Hypertrophic Cardiomyopathy

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Variations for Nexn-Related Familial Hypertrophic Cardiomyopathy

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Expression for genes affiliated with Nexn-Related Familial Hypertrophic Cardiomyopathy

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Search GEO for disease gene expression data for Nexn-Related Familial Hypertrophic Cardiomyopathy.

Pathways for genes affiliated with Nexn-Related Familial Hypertrophic Cardiomyopathy

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GO Terms for genes affiliated with Nexn-Related Familial Hypertrophic Cardiomyopathy

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Sources for Nexn-Related Familial Hypertrophic Cardiomyopathy

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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