Dentin dysplasia
General Information (adopted from Orphanet):
| Synonyms, Signs: |
DD |
| Number of Symptoms | 4 |
| OrphanetNr: | 1653 |
| OMIM Id: |
|
| ICD-10: |
K00.5 |
| UMLs: |
C0011430 |
| MeSH: |
D003805 |
| MedDRA: |
|
| Snomed: |
109492001 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant [Orphanet] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Hereditary dentin defect
-Rare genetic disease -Rare odontologic disease |
Symptom Information:
|
|
(HPO:0010299) | Abnormality of dentin | Very frequent [Orphanet] | 9 / 7739 | |||
|
|
(HPO:0006482) | Abnormality of dental morphology | Very frequent [Orphanet] | 81 / 7739 | |||
|
|
(HPO:0100777) | Exostoses | Frequent [Orphanet] | 32 / 7739 | |||
|
|
(HPO:0011001) | Increased bone mineral density | Very frequent [Orphanet] | 78 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|