Disease #03504 (OI6 (osteogenesis imperfecta, type VI (OI6)), OMIM:613982)
Official abbreviation |
OI6 |
Name |
osteogenesis imperfecta, type VI (OI6) |
OMIM ID |
613982 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
SERPINF1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-05-16 12:55:18 +02:00 (CEST) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|