Gene table: search width pubmed_id = 9697706


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Myofibrillar myopathy 1 - (AD)
5.1
9697706
DES (2q35)
Desmin
* Desmin-related myopathy - DRM
* Limb-Girdle, Muscular dystrophy, type 2R - LGMD2R
* Dilated cardiomyopathy, 1I - CMD1I
* Arrhythmogenic right ventricular dysplasia with myofibrillar myopathy - ARVD7
* Myofibrillar myopathy 1 - MFM1
* Myopathy, cardiomyopathy and congenital myasthenic syndrome
* Limb girdle muscular dystrophy 1E (autosomal dominant) - LGMD1E