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Deafness - oligodontia

Orpha number ORPHA3230
Synonym(s) -
Prevalence -
Inheritance -
Age of onset -
ICD-10 -
ICD-O -
OMIM
UMLS
  • C1857333
MeSH
  • C538049
MedDRA -

Summary

This syndrome is characterised by sensorineural hearing loss and oligodontia/hypodontia. It has been described in two pairs of siblings and in one isolated case. Dizziness was reported in one of the pairs of siblings. Transmission appears to be autosomal recessive.


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