Cardiomyopathy, Familial Hypertrophic, 12 (CMH12)

Alias:
Hypertrophic Cardiomyopathy 12
Cmh12
Cardiomyopathy, Hypertrophic, Familial, Type 12
Cardiomyopathy Familial Hypertrophic 12
Cardiomyopathy, Hypertrophic, 12
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cardiomyopathy, Familial Hypertrophic, 12, also known as hypertrophic cardiomyopathy 12, is related to type 1 diabetes mellitus 12 and endometrial disease. An important gene associated with Cardiomyopathy, Familial Hypertrophic, 12 is CSRP3 (Cysteine And Glycine Rich Protein 3), and among its related pathways/superpathways are Innate Immune System and Defensins. Affiliated tissues include heart and breast, and related phenotypes are hypertrophic cardiomyopathy and ventricular septal hypertrophy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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5
17
9

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

Name
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
Year
IF
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