OBO ID: DOID:4154
Term Name: dentinogenesis imperfecta Search Ontology:
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:
Ontology: Human Disease   ( DOID:4154 )
Relationships
is a type of:
OTHER dentinogenesis imperfecta PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DSPP Dentinogenesis imperfecta, Shields type III
Dentinogenesis imperfecta, Shields type II
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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