Cardiomyopathy, Familial Hypertrophic, 7 (CMH7)

Alias:
Hypertrophic Cardiomyopathy 7
Cmh7
Cardiomyopathy, Hypertrophic, Familial, Type 7
Cardiomyopathy, Familial Hypertrophic 7
Cardiomyopathy, Hypertrophic, 7
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cardiomyopathy, Familial Hypertrophic, 7, also known as hypertrophic cardiomyopathy 7, is related to familial isolated dilated cardiomyopathy and intrinsic cardiomyopathy. An important gene associated with Cardiomyopathy, Familial Hypertrophic, 7 is TNNI3 (Troponin I3, Cardiac Type). Affiliated tissues include heart and heart-ventricle, and related phenotypes are atrial fibrillation and hypertrophic cardiomyopathy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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7
25
31

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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