SEMA6A, semaphorin 6A, 57556

N. diseases: 211; N. variants: 4
Disease: Ullrich congenital muscular dystrophy 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0410179
Disease: Ullrich congenital muscular dystrophy 1
Ullrich congenital muscular dystrophy 1 		0.010 Biomarker disease BEFREE Clinically, the disorder shares many features with the kyphoscoliotic type of EDS (EDS VIA) and Ullrich congenital muscular dystrophy. 22265013 2012