DNAH11, dynein axonemal heavy chain 11, 8701

N. diseases: 110; N. variants: 109
Disease: Heterotaxy Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		0.210 GeneticVariation disease BEFREE DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome. 31040315 2019
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		0.210 Biomarker disease MGD