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
  • GARD:6258
  • ICD10CM:K00.5
  • MESH:D003811
  • MIM:125490
  • MIM:125500
  • NCI:C84667
  • ORDO:49042
  • SNOMEDCT_US_2023_03_01:367461002
  • UMLS_CUI:C0011436
Ontology
Human Disease   ( DOID:4154 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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