Congenital Myopathy 7b, Myosin Storage, Autosomal Recessive (CMYP7B)

Alias:
Myopathy, Myosin Storage, Autosomal Recessive
Msmb
Myopathy, Hyaline Body, Autosomal Recessive
Cmyp7b
Autosomal Recessive Myosin Storage Myopathy
Autosomal Recessive Hyaline Body Myopathy
Congenital Myopathy 7b
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Myopathy 7b, Myosin Storage, Autosomal Recessive, also known as myopathy, myosin storage, autosomal recessive, is related to congenital myopathy 7a, myosin storage, autosomal dominant and myopathy. An important gene associated with Congenital Myopathy 7b, Myosin Storage, Autosomal Recessive is MYH7 (Myosin Heavy Chain 7). Affiliated tissues include skeletal muscle and lung, and related phenotypes are scoliosis and short stature
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
8
12

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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