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Agent Commons
Collaborative Research
Diseases
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Auditory system disorder
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Inherited auditory system disease
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Nonsyndromic genetic hearing loss
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Autosomal dominant nonsyndromic hearing loss
Hearing loss, autosomal dominant 34, with or without inflammation
rare
Identifiers
MONDO:0033261
OMIM:617772
Causal genes
NLRP3
Part of
Autosomal dominant nonsyndromic hearing loss
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