Disease #01253 (CCD (dysplasia, cleidocranial (CCD)), OMIM:119600)
| Official abbreviation |
CCD |
| Name |
dysplasia, cleidocranial (CCD) |
| OMIM ID |
119600 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
RUNX2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|