Fatal Congenital Hypertrophic Cardiomyopathy Due to Glycogen Storage Disease

Alias:
Fatal Congenital Hypertrophic Cardiomyopathy Due to Glycogenosis
Fatal Congenital Hypertrophic Cardiomyopathy Due to Gsd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Fatal Congenital Hypertrophic Cardiomyopathy Due to Glycogen Storage Disease, also known as fatal congenital hypertrophic cardiomyopathy due to glycogenosis, is related to glycogen storage disease of heart, lethal congenital. An important gene associated with Fatal Congenital Hypertrophic Cardiomyopathy Due to Glycogen Storage Disease is PRKAG2 (Protein Kinase AMP-Activated Non-Catalytic Subunit Gamma 2). Affiliated tissues include skeletal muscle.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
<1/1000000
1
10
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Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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No data available

Related Drugs

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No data available

Disease Model

Category
Name
MGI
Related Gene
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Publications
No data available

References Literature

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