Disease #00332 (CILD (dyskinesia, ciliary, primary (CILD)))
Official abbreviation |
CILD |
Name |
dyskinesia, ciliary, primary (CILD) |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
219 |
Phenotype entries for this disease |
211 |
Associated with 9 genes |
C21orf59, CCDC164, CCDC39, DNAAF3, DNAH1, DNAH5, HEATR2, HYDIN, TTC12 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-02-21 12:58:05 +01:00 (CET) |
Date last edited |
2015-03-31 17:58:20 +02:00 (CEST) |
Individuals
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