Cardiomyopathy, Familial Hypertrophic, 20 (CMH20)

Alias:
Hypertrophic Cardiomyopathy 20
Cmh20
Cardiomyopathy, Hypertrophic, Familial, Type 20
Cardiomyopathy Familial Hypertrophic 20
Cardiomyopathy, Hypertrophic, 20
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cardiomyopathy, Familial Hypertrophic, 20, also known as hypertrophic cardiomyopathy 20, is related to urinary tract infection and cardiomyopathy, dilated, 1cc. An important gene associated with Cardiomyopathy, Familial Hypertrophic, 20 is NEXN (Nexilin F-Actin Binding Protein), and among its related pathways/superpathways are Platelet Aggregation Inhibitor Pathway, Pharmacodynamics and FOXA2 and FOXA3 transcription factor networks. Affiliated tissues include heart and lung, and related phenotypes are hypertrophic cardiomyopathy and left ventricular hypertrophy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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6
74
12

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
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