LEMD3, LEM domain containing 3, 23592

N. diseases: 112; N. variants: 5
Disease: Hyperostosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020492
Disease: Hyperostosis
Hyperostosis 		0.110 GeneticVariation disease BEFREE Mutations in MAN1, a protein of the nuclear envelope, cause bone phenotypes characterized by hyperostosis. 28449239 2017
CUI: C0020492
Disease: Hyperostosis
Hyperostosis 		0.110 Biomarker disease HPO