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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|