Disease #05746 (OPTA (osteopetrosis, autosomal dominant (OPTA)))
| Official abbreviation |
OPTA |
| Name |
osteopetrosis, autosomal dominant (OPTA) |
| OMIM ID |
- |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 2 genes |
CLCN7, LRP5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-05-18 09:27:27 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
|