Disease #05747 (OPTB (osteopetrosis, autosomal recessive (OPTB)))
| Official abbreviation |
OPTB |
| Name |
osteopetrosis, autosomal recessive (OPTB) |
| OMIM ID |
- |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
10 |
| Phenotype entries for this disease |
10 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-05-18 09:28:28 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|