eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | situs ambiguus |
| Comorbidity | C0022658|kidney disease |
| Sentences | 2 |
| PubMedID- 22705113 | Autosomal dominant polycystic kidney disease with situs inversus. |
| PubMedID- 23515530 | Mutations in inversin cause nephronophthisis type ii, an autosomal recessive form of polycystic kidney disease associated with situs inversus, dilatation, and kidney cyst formation. |
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