DEAFNESS, AUTOSOMAL DOMINANT 16
General Information (adopted from Orphanet):
Synonyms, Signs: |
DFNA16 |
Number of Symptoms | 3 |
OrphanetNr: | |
OMIM Id: |
603964
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ICD-10: |
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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 inheritance [Omim] |
Age of onset: |
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Disease classification (adopted from Orphanet):
Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0008615) | Adult onset sensorineural hearing impairment | 4 / 7739 | ||||
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(HPO:0000360) | Tinnitus | rare [HPO:skoehler] | 29 / 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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Additional Information:
Clinical Description OMIM |
Fukushima et al. (1999) reported a family in which 13 members over 4 generations had a form of autosomal dominant nonsyndromic hearing loss, designated DFNA16, in which the phenotype included rapidly progressing and fluctuating hearing loss that appeared ... |