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
|