Disease #03855 (OI15 (osteogenesis imperfecta, type XV (OI15)), OMIM:615220)
| Official abbreviation |
OI15 |
| Name |
osteogenesis imperfecta, type XV (OI15) |
| OMIM ID |
615220 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
WNT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-05-16 21:50:02 +02:00 (CEST) |
Individuals
|