Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4649
Gene Symbol: MYO9A
MYO9A
CUI: C0751884
Disease: Congenital Myasthenic Syndromes, Presynaptic
Congenital Myasthenic Syndromes, Presynaptic 		0.300 GermlineCausalMutation ORPHANET Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome. 27259756

2016