Details of Disease

General Information of Disease (ID: DIS2FXY9)

Disease Name Obsolete congenital myopathy with excess of thin filaments
Disease Hierarchy
DIS01GPL: Grass pollen hypersensitivity
DIS2FXY9: Obsolete congenital myopathy with excess of thin filaments

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ACTA1 OTOVGLPG Definitive Semidominant [1]
------------------------------------------------------------------------------------

References

1 Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy. Nat Genet. 1999 Oct;23(2):208-12. doi: 10.1038/13837.