MEGF10, multiple EGF like domains 10, 84466

N. diseases: 41; N. variants: 17
Disease: Esophageal Dysphagia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0267072
Disease: Esophageal Dysphagia
Esophageal Dysphagia 		0.300 Biomarker disease CTD_human Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD). 22101682 2011