Disease #01483 (OPTA2 (osteopetrosis, autosomal dominant, type 2), OMIM:166600)
| Official abbreviation |
OPTA2 |
| Name |
osteopetrosis, autosomal dominant, type 2 |
| OMIM ID |
166600 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
CLCN7 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-05-05 09:47:20 +02:00 (CEST) |
Individuals
|