Familial Isolated Restrictive Cardiomyopathy

Alias:
Familial or Idiopathic Restrictive Cardiomyopathy
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Familial Isolated Restrictive Cardiomyopathy, also known as familial or idiopathic restrictive cardiomyopathy, is related to myopathy, myofibrillar, 1 and cardiomyopathy, familial restrictive, 2. An important gene associated with Familial Isolated Restrictive Cardiomyopathy is FLNC (Filamin C), and among its related pathways/superpathways are Cardiac conduction and Cytoskeletal Signaling. Affiliated tissues include heart, and related phenotypes are abnormal left ventricular function and right atrial enlargement
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
All ages
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6
49
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Medical Symptom

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

Gene & Mutation

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Mutations
No data available

Related Drugs

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CAS Number
Status
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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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