Disease #05891 (OI20 (osteogenesis imperfecta, type XX (OI20)), OMIM:618644)
| Official abbreviation |
OI20 |
| Name |
osteogenesis imperfecta, type XX (OI20) |
| OMIM ID |
618644 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
MESDC2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-01-12 17:22:55 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|