Congenital Myopathy 2a, Typical, Autosomal Dominant (CMYP2A)

Alias:
Nemaline Myopathy 3
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
Nemaline Myopathy 3, Autosomal Dominant or Recessive
Nem3
Cmyp2a
Nemaline Myopathy 3, with Intranuclear Rods
Nemaline Myopathy 3 with Intranuclear Rods
Myopathy, Actin, Congenital, with Cores
Actin Myopathy Congenital with Cores
Acta1-Related Nemaline Myopathy
Actin-Accumulation Myopathy
Actin Accumulation Myopathy
Myopathy, Nemaline, Type 3
Nemaline Myopathy, Type 3
Congenital Myopathy 2a
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Myopathy 2a, Typical, Autosomal Dominant, also known as nemaline myopathy 3, is related to van der woude syndrome and actin-accumulation myopathy, and has symptoms including waddling gait, facial paresis and generalized muscle weakness. An important gene associated with Congenital Myopathy 2a, Typical, Autosomal Dominant is ACTA1 (Actin Alpha 1, Skeletal Muscle), and among its related pathways/superpathways are DNA repair pathways, full network and Cytoprotection by HMOX1. Affiliated tissues include skeletal muscle, and related phenotypes are hyperreflexia and hypertonia
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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6
49
92

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
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IF
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