Cardiomyopathy, Familial Restrictive, 1 (RCM1)

Alias:
Rcm1
Restrictive Cardiomyopathy 1
Cardiomyopathy, Restrictive, Familial, Type 1
Cardiomyopathy, Familial Restrictive 1
Familial Restrictive Cardiomyopathy 1
Rcm-1
Rcm
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cardiomyopathy, Familial Restrictive, 1, also known as rcm1, is related to restrictive cardiomyopathy and cardiomyopathy, familial hypertrophic, 1. An important gene associated with Cardiomyopathy, Familial Restrictive, 1 is TNNI3 (Troponin I3, Cardiac Type), and among its related pathways/superpathways are tRNA processing and tRNA-uridine 2-thiolation (cytoplasmic). Affiliated tissues include heart and whole blood, and related phenotypes are left ventricular hypertrophy and left atrial enlargement
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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15
79
15

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

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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
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IF
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