dentin dysplasia
MONDO:0015613Mondo
Findings
No curated finding names dentin dysplasia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0015613), read 2026-09-29. CC BY 4.0.
Features
4 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal dental enamel morphologyHPOHP:0000682
- Very frequent (80% to 99% of cases)
- Abnormal dental morphologyHPOHP:0006482
- Very frequent (80% to 99% of cases)
- Increased bone mineral densityHPOHP:0011001
- Very frequent (80% to 99% of cases)
- ExostosesHPOHP:0100777
- Frequent (30% to 79% of cases)
Where it sits
- A kind of
- Narrower terms (2)
Other names
1 name
Resolves to: dentin dysplasia
- Also called
- DD