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
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