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
|
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