Disease #00028 (CILD15 (dyskinesia, ciliary, primary, type 15 (CILD-15)), OMIM:613808)
| Official abbreviation |
CILD15 |
| Name |
dyskinesia, ciliary, primary, type 15 (CILD-15) |
| OMIM ID |
613808 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
28 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CCDC40 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-08-20 12:34:48 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|