Myofibrillar Myopathy 11 (MFM11)

Alias:
Mfm11
Myopathy, Congenital, with Eccentric Cores
Myopathy, Myofibrillar, 11
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Myofibrillar Myopathy 11, is also known as mfm11. An important gene associated with Myofibrillar Myopathy 11 is UNC45B (Unc-45 Myosin Chaperone B). Affiliated tissues include skeletal muscle, and related phenotypes are feeding difficulties in infancy and decreased fetal movement
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
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
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IF
No Data Found!
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