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| Term | osteogenesis imperfecta type 5 | ID (Ontology) | DOID:0110344 (Human Disease) |
| Definition | An osteogenesis imperfecta that has_material_basis_in mutation in the IFITM5 gene on chromosome 11p15. | ||
| Also Known As | "OI5" ; "osteogenesis imperfecta type V" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ osteochondrodysplasia | |__osteogenesis imperfecta_____| osteogenesis imperfecta type 5 |
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| Is a |
autosomal dominant disease osteogenesis imperfecta |
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External Crossreferences & Linkouts
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GARD:8699 ICD10CM:Q78.0 MIM:610967 |
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