Nemaline Myopathy 5c, Autosomal Dominant (NEM5C)

Alias:
Nem5c
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Nemaline Myopathy 5c, Autosomal Dominant, is also known as nem5c. An important gene associated with Nemaline Myopathy 5c, Autosomal Dominant is TNNT1 (Troponin T1, Slow Skeletal Type). Affiliated tissues include skeletal muscle, and related phenotypes are nemaline bodies and high palate

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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1
6
4

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
No Data Found!
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