FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term dentin dysplasia ID (Ontology) DOID:701 (Human Disease)
Definition A teeth hard tissue disease characterized by presence of normal enamel but atypical dentin with abnormal pulpal morphology.
Also Known As "Dentinal dysplasia"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 dentin dysplasia       1
 for disease ribbon | dentin dysplasia       1
 model of | dentin dysplasia       1
Spanning Tree (Parents/Children)
Only view relationship: 
  tooth disease
   |__teeth hard tissue disease
       |__dentin dysplasia  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a teeth hard tissue disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Dentinal dysplasia" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:K00.5
MESH:D003805
MIM:125400
MIM:125420
ORDO:1635
SNOMEDCT_US_2023_03_01:109492001
UMLS_CUI:C0011430