Disease #02684 (OPTA1 (osteopetrosis, autosomal dominant, type 1), OMIM:607634)
Official abbreviation |
OPTA1 |
Name |
osteopetrosis, autosomal dominant, type 1 |
OMIM ID |
607634 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
LRP5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2025-05-05 09:47:03 +02:00 (CEST) |
Individuals
|