Cardiomyopathy, Infantile Hypertrophic (CMHI)

Alias:
Infantile Hypertrophic Cardiomyopathy
Cmhi
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cardiomyopathy, Infantile Hypertrophic, also known as infantile hypertrophic cardiomyopathy, is related to combined oxidative phosphorylation deficiency 10 and mitochondrial disease. An important gene associated with Cardiomyopathy, Infantile Hypertrophic is MT-ATP8 (Mitochondrially Encoded ATP Synthase Membrane Subunit 8), and among its related pathways/superpathways are Metabolism and Processing of Capped Intron-Containing Pre-mRNA. Affiliated tissues include heart and nk cells, and related phenotypes are muscle and cellular
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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22
98
1

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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