Cardiomyopathy, Dilated, 1kk (CMD1KK)
Alias:
Cardiomyopathy, Familial Restrictive, 4
Dilated Cardiomyopathy 1kk
Cmd1kk
Cardiomyopathy, Familial Hypertrophic, 22
Cardiomyopathy, Hypertrophic, 22
Familial Hypertrophic Cardiomyopathy 22
Cardiomyopathy, Familial Restrictive 4
Cardiomyopathy, Dilated, Type 1kk
Cmh22
Rcm4
Basic Information
Medical Symptom
Gene & Mutation
Drugs
Disease Model
References
Cardiomyopathy, Dilated, 1kk, also known as cardiomyopathy, familial restrictive, 4, is related to cardiomyopathy, dilated, 1a and distal hereditary motor neuronopathy type 2a. An important gene associated with Cardiomyopathy, Dilated, 1kk is MYPN (Myopalladin), and among its related pathways/superpathways are O-linked glycosylation of mucins and Defective DPM3 causes DPM3-CDG. Affiliated tissues include heart and heart-ventricle, and related phenotypes are dilated cardiomyopathy and ventricular septal hypertrophy
Basic Information
Inheritance
Age Of Onset
Prevalence
Related Gene
Related Models
Reference
MALACARDS
AD
Unknown
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1
4
8
Medical Symptom
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Categorization
Description
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Orphanet Frequency
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No data available
Gene & Mutation
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No data available
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Name
MGI
Related Gene
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No data available
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No Data Found!
Comparison
Al agent
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