Search Ontology:
Human Disease
osteogenesis imperfecta type 13
- Term ID
- DOID:0110342
- Synonyms
-
- OI13
- osteogenesis imperfecta type XIII
- Definition
- An osteogenesis imperfecta that has_material_basis_in mutation in the BMP1 gene on chromosome 8p21. https://www.ncbi.nlm.nih.gov/pubmed/22052668
- References
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- ICD10CM:Q78.0
- MIM:614856
- Ontology
- Human Disease ( DOID:0110342 )
- is a type of
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Other Pages
Genes Involved
Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
---|---|---|---|---|
BMP1 | Osteogenesis imperfecta, type XIII | osteogenesis imperfecta type 13 | 614856 |
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Zebrafish Models
Fish | Conditions | Disease | Citation |
---|---|---|---|
bmp1asa2416/sa2416 | standard conditions | osteogenesis imperfecta type 13 | 2 publications |
1 - 1 of 1
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