Congenital Myopathy 24 (CMYP4)

Alias:
Nemaline Myopathy 11, Autosomal Recessive
Nem11
Mypn-Related Myopathy
Nemaline Myopathy 11
Cmyp4
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Myopathy 24, also known as nemaline myopathy 11, autosomal recessive, is related to nemaline myopathy 11 and nemaline myopathy. An important gene associated with Congenital Myopathy 24 is MYPN (Myopalladin). Affiliated tissues include skeletal muscle and heart, and related phenotypes are muscle weakness and type 1 muscle fiber predominance
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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1
5
2

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

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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
Journal
Year
IF
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