DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: CNS metastases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0686377
Disease: CNS metastases
CNS metastases 		0.010 GeneticVariation phenotype BEFREE Mutations affecting the correct expression of these tissue-specific isoforms have been associated with the CNS involvement common in DMD. 14636778 2003