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dentin dysplasia
Disease Summary
Associated Targets (4)
Tbio
3
Tchem
1
Mondo Description Dentin dysplasia (DD) is a rare disorder belonging to the group of hereditary dentin defects and is characterized by abnormal dentin structure and root development resulting in abnormal tooth development. It encompasses two subtypes: DD type I and DD type II.
Disease Ontology Description A teeth hard tissue disease characterized by presence of normal enamel but atypical dentin with abnormal pulpal morphology.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:701
MESH:D003805
Orphanet:1653
SCTID:109492001
MONDO:0015613
High level summary of knowledge for a disease, including descriptions and datasource references.