Disease #02998 (OI5 (osteogenesis imperfecta, type V (OI5)), OMIM:610967)
| Official abbreviation |
OI5 |
| Name |
osteogenesis imperfecta, type V (OI5) |
| OMIM ID |
610967 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
6 |
| Associated with 1 gene |
IFITM5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-05-16 09:24:20 +02:00 (CEST) |
Individuals
|