nonsyndromic deafness
Sign in to saveAlso known as nonsyndromic hearing loss, nonsyndromic hereditary hearing loss, Familial deafness, Non-syndromic genetic deafness, Isolated genetic deafness
auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms
In the Vinony graph
Vinony's link graph records 295 inbound references to nonsyndromic deafness, and connects out to hereditary spherocytosis, epidermolysis bullosa simplex and hearing loss.
Vinony files it under Channelopathies, Deafness and Mitochondrial diseases.
Vinony links it to 5 Wikipedia language editions.
Connections
hereditary spherocytosis
Entity
epidermolysis bullosa simplex
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hearing loss
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Charcot–Marie–Tooth disease
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dominance
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hereditary elliptocytosis
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Axenfeld-Rieger syndrome
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epidermolysis bullosa dystrophica
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SLC17A8
Gene
deoxyribonucleic acid
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bone
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deafness
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natural environment
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Parkinson's disease
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mitochondrion
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digital object identifier
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International Standard Serial Number
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hearing
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mutation
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magnetic resonance imaging
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