Disease #04672 (OI17 (osteogenesis imperfecta, type XVII (OI17)), OMIM:616507)
| Official abbreviation |
OI17 |
| Name |
osteogenesis imperfecta, type XVII (OI17) |
| OMIM ID |
616507 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
SPARC |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2021-05-16 13:25:25 +02:00 (CEST) |
Individuals
|