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
|