Disease #05935 (OI19 (osteogenesis imperfecta type XIX (OI19)), OMIM:301014)
| Official abbreviation |
OI19 |
| Name |
osteogenesis imperfecta type XIX (OI19) |
| OMIM ID |
301014 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
MBTPS2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-05-16 21:41:43 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
|