Search Ontology:
Human Disease

dentinogenesis imperfecta

Term ID
DOID:4154
Synonyms
Definition
A tooth disease characterized by discolored, opalescent teeth that has_material_basis_in mutation in the DSPP gene on chromosome 4q22. https://pubmed.ncbi.nlm.nih.gov/19021896/
References
(all 9)
Ontology
Human Disease   ( DOID:4154 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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