Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.710 GeneticVariation disease BEFREE Mutations of Dynamin 2 (DNM2) are responsible for several forms of neuromuscular disorder such as centronuclear myopathy, Charcot-Marie-Tooth disease (CMT) dominant intermediate type B, CMT 2M, and lethal congenital contracture syndrome 5. 28971531 2018
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.710 GeneticVariation disease UNIPROT Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome. 23092955 2013
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.710 GermlineCausalMutation disease ORPHANET Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome. 23092955 2013
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.710 Biomarker disease GENOMICS_ENGLAND Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome. 23092955 2013
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.710 Biomarker disease GENOMICS_ENGLAND Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease. 15731758 2005
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.710 Biomarker disease CTD_human
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.710 CausalMutation disease CLINVAR