Taurodontism
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 4 |
| OrphanetNr: | 3289 |
| OMIM Id: |
272700
|
| ICD-10: |
K00.2 |
| UMLs: |
C0266039 |
| MeSH: |
C536946 |
| MedDRA: |
|
| Snomed: |
51744007 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
|
| Age of onset: |
|
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Rare odontal or periodontal disorder
-Rare genetic disease -Rare odontologic disease |
Symptom Information:
|
|
(HPO:0000682) | Abnormality of dental enamel | Occasional [Orphanet] | 102 / 7739 | |||
|
|
(HPO:0000679) | Taurodontia | Occasional [Orphanet] | 27 / 7739 | |||
|
|
(OMIM) | Root deep in alveolar bone | 1 / 7739 | ||||
|
|
(OMIM) | Large dental pulp chambers | 1 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|