loading...| Preferred Name |
Kartagener Syndrome [Disease/Finding] |
|
| Synonyms |
Ciliary Dyskinesia, Primary |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001731 |
|
| altLabel |
Ciliary Dyskinesia, Primary Kartagener's Triad Kartagener Syndrome Primary Ciliary Dyskinesia Kartagener's Syndrome Siewert Syndrome Kartagener Triad Dextrocardia, Bronchiectasis, and Sinusitis Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus Ciliary Dyskinesia, Primary, 1 Polynesian Bronchiectasis |
|
| cui |
C0022521 C4317124 |
|
| MESH DEFINITION |
An autosomal recessive disorder characterized by a triad of DEXTROCARDIA; INFERTILITY; and SINUSITIS. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and CILIA in the respiratory and the reproductive tracts. |
|
| MESH DUI |
D007619 |
|
| MeSH name |
Kartagener Syndrome |
|
| MESH UI |
M0011929 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000001731 |
|
| NUI |
N0000001731 |
|
| prefLabel |
Kartagener Syndrome [Disease/Finding] |
|
| SNOMED CID |
42402006 |
|
| tui |
T047 |
|
| subClassOf |