Congenital Myopathy 15 (CMYP15)

Alias:
Myopathy, Congenital, with Neonatal Respiratory Insufficiency
Cmyp15
Myonri
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Myopathy 15, is also known as myopathy, congenital, with neonatal respiratory insufficiency. An important gene associated with Congenital Myopathy 15 is TNNC2 (Troponin C2, Fast Skeletal Type). Affiliated tissues include skeletal muscle and eye, and related phenotypes are muscle weakness and weakness of facial musculature
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Basic Information

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

Medical Symptom

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

Gene & Mutation

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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
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IF
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