eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | kartagener syndrome |
| Comorbidity | C0024115|pulmonary disease |
| Sentences | 1 |
| PubMedID- 21926394 | Primary ciliary dyskinesia (pcd) is an autosomal recessive, rare, genetically heterogeneous condition characterized by oto-sino-pulmonary disease together with situs abnormalities (kartagener syndrome) owing to abnormal ciliary structure and function. |
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