Disease #02998 (OI5 (osteogenesis imperfecta, type V (OI5)), OMIM:610967)
Official abbreviation |
OI5 |
Name |
osteogenesis imperfecta, type V (OI5) |
OMIM ID |
610967 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
8 |
Phenotype entries for this disease |
6 |
Associated with 1 gene |
IFITM5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-05-16 09:24:20 +02:00 (CEST) |
Individuals
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