DNAH11, dynein axonemal heavy chain 11, 8701

N. diseases: 110; N. variants: 109
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4025885
Disease: Abnormality of the uvula
Abnormality of the uvula
0.100 GeneticVariation phenotype CLINVAR
CUI: C4025885
Disease: Abnormality of the uvula
Abnormality of the uvula
0.100 CausalMutation phenotype CLINVAR