Cardiomyopathy, Familial Hypertrophic, 9 (CMH9)

Alias:
Hypertrophic Cardiomyopathy 9
Cmh9
Cardiomyopathy, Hypertrophic, Familial, Type 9
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cardiomyopathy, Familial Hypertrophic, 9, also known as hypertrophic cardiomyopathy 9, is related to hypertrophic cardiomyopathy and cardiomyopathy, familial hypertrophic, 1. An important gene associated with Cardiomyopathy, Familial Hypertrophic, 9 is TTN (Titin), and among its related pathways/superpathways is Defective DPM3 causes DPM3-CDG. Affiliated tissues include heart and cardiac myocytes, and related phenotype is hypertrophic cardiomyopathy.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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8
49
10

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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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
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IF
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