Dentinogenesis Imperfecta
Disease ID: disease_node_2440
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| Dbxref | GARD:6258, ICD10CM:K00.5, MESH:D003811, MIM:125490, MIM:125500, NCI:C84667, ORDO:49042, SNOMEDCT_US_2023_03_01:367461002, UMLS_CUI:C0011436 |
|---|---|
| Subclassof | DOID_0050736, DOID_1091 |
| Data Source | DOID, MESH |
| Mesh Id | D003811 |
| Mesh Label | Dentinogenesis Imperfecta |
| Mesh Subclassof | D014071 |
| Doid Label | dentinogenesis imperfecta |
| Doid Description | A tooth disease characterized by discolored, opalescent teeth that has_material_basis_in mutation in the DSPP gene on chromosome 4q22. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_2440 |
| Doid Id | DOID_4154 |
| Label | Dentinogenesis Imperfecta |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Tooth Diseases(ID:disease_node_7477) (Disease)