Oligodontia
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Selective tooth agenesis |
| Number of Symptoms | 7 |
| OrphanetNr: | 99798 |
| OMIM Id: |
106600
150400 313500 604625 610926 613097 |
| ICD-10: |
K00.0 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant Autosomal recessive X-linked recessive [Orphanet] |
| Age of onset: |
Childhood [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Rare odontal or periodontal disorder
-Rare genetic disease -Rare odontologic disease |
Symptom Information:
|
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(HPO:0000691) | Microdontia | Very frequent [Orphanet] | 104 / 7739 | |||
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(HPO:0000308) | Microretrognathia | Very frequent [Orphanet] | 78 / 7739 | |||
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(HPO:0000668) | Hypodontia | 81 / 7739 | ||||
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(HPO:0009804) | Reduced number of teeth | Very frequent [Orphanet] | 137 / 7739 | |||
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(HPO:0006482) | Abnormality of dental morphology | Very frequent [Orphanet] | 81 / 7739 | |||
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(HPO:0000271) | Abnormality of the face | Very frequent [Orphanet] | 108 / 7739 | |||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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