DNAH11, dynein axonemal heavy chain 11, 8701

N. diseases: 110; N. variants: 109
Disease: Congenital atresia of nasopharynx ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		0.200 Biomarker disease MGD Abnormal nodal flow precedes situs inversus in iv and inv mice. 10549278 1999