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| General Information | |||
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| Term | dentinogenesis imperfecta | ID (Ontology) | DOID:4154 (Human Disease) |
| Definition | A tooth disease characterized by discolored, opalescent teeth that has_material_basis_in mutation in the DSPP gene on chromosome 4q22. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ mouth disease | |__tooth disease_______________| dentinogenesis imperfecta |
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Relationships
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| Is a |
autosomal dominant disease tooth disease |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:6258 ICD10CM:K00.5 MESH:D003811 MIM:125490 MIM:125500 NCI:C84667 ORDO:49042 SNOMEDCT_US_2023_03_01:367461002 UMLS_CUI:C0011436 |
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