Preferred Name | dentinogenesis imperfecta | |
Synonyms |
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Definitions |
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]. |
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ID |
http://purl.obolibrary.org/obo/DOID_4154 |
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comment |
OMIM mapping confirmed by DO. [SN]. |
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database_cross_reference |
OMIM:125490 SNOMEDCT_US_2023_03_01:367461002 ICD10CM:K00.5 OMIM:125500 MESH:D003811 UMLS_CUI:C0011436 GARD:6258 NCI:C84667 ORDO:49042 |
|
definition |
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]. |
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has material basis in | ||
has_obo_namespace |
disease_ontology |
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id |
DOID:4154 |
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in_subset | ||
label |
dentinogenesis imperfecta |
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notation |
DOID:4154 |
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note |
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]. |
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preferred label |
dentinogenesis imperfecta |
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prefLabel |
dentinogenesis imperfecta |
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subClassOf |