Familial progressive vestibulocochlear dysfunction
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Number of Symptoms
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3
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OrphanetNr:
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1767
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OMIM Id:
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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:
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Prevalence:
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No data available.
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Inheritance:
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Autosomal dominant inheritance
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Age of onset:
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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No data available.
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1
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(HPO:0000407)
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Sensorineural hearing impairment |
Very frequent [Orphanet]
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524 / 7739
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2
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(HPO:0011390)
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Morphological abnormality of the inner ear |
Very frequent [Orphanet]
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21 / 7739
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3
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(HPO:0001288)
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Gait disturbance |
Very frequent [Orphanet]
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318 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |