Osteogenesis Imperfecta Type 6
Disease ID: disease_node_15618
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| Dbxref | GARD:8700, ICD10CM:Q78.0, MIM:613982 |
|---|---|
| Subclassof | DOID_12347, DOID_0050177 |
| Data Source | DOID |
| Synonyms | OI6, osteogenesis imperfecta type VI |
| Doid Label | osteogenesis imperfecta type 6 |
| Doid Description | An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINF1 gene on chromosome 17p13.3. |
| Disease Node Id | disease_node_15618 |
| Doid Id | DOID_0110350 |
| Disease Has Basis In | SO_0000704 |
| Label | Osteogenesis Imperfecta Type 6 |
- Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease)