DES, desmin, 1674

N. diseases: 330; N. variants: 63
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
0.040 Biomarker group BEFREE LVhMyoD transduced cells readily formed striated, multinucleate myotubes expressing a wide range of genes associated with muscular dystrophy (dystrophin, dysferlin, sarcoglycans, caveolin-3) and congenital myopathy (nebulin, actin, desmin, tropomyosin, troponin). 17303423 2007
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
0.040 Biomarker group BEFREE Although not initially included within the congenital myopathies, desmin-related or myofibrillar myopathies are described here because they are closely related to other congenital myopathies with intracytoplasmic inclusions. 12351999 2002
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
0.040 AlteredExpression group BEFREE Desmin is highly expressed in immature muscle fibers, both during fetal life and regeneration as well as in certain congenital myopathies, together with vimentin. 7565929 1995
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
0.040 Biomarker group BEFREE The exclusive appearance of desmin, ubiquitin and dystrophin positive plaques in muscle specimens from 5 children emphasize the uniqueness of these plaques as well as this special form of a congenital myopathy. 7561954 1995