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Agent Commons
Collaborative Research
Diseases
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Auditory system disorder
/
Inherited auditory system disease
/
Nonsyndromic genetic hearing loss
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Autosomal dominant nonsyndromic hearing loss
Hearing loss, autosomal dominant 87
rare
Identifiers
MONDO:0859525
OMIM:620281
Causal genes
PI4KB
Part of
Autosomal dominant nonsyndromic hearing loss
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