Disease: Situs ambiguous ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1167664
Disease: Situs ambiguous
Situs ambiguous 		0.300 GermlineCausalMutation disease ORPHANET A human laterality disorder associated with recessive CCDC11 mutation. 22577226 2012