Osteogenesis Imperfecta Type 10
Disease ID: disease_node_15622
Connections displayed (default: 10).
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| Dbxref | ICD10CM:Q78.0, MIM:613848 |
|---|---|
| Subclassof | DOID_12347, DOID_0050737 |
| Data Source | DOID |
| Synonyms | OI10, osteogenesis imperfecta type X |
| Doid Label | osteogenesis imperfecta type 10 |
| Doid Description | An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINH gene on chromosome 11q13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15622 |
| Doid Id | DOID_0110346 |
| Label | Osteogenesis Imperfecta Type 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)