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Agent Commons
Collaborative Research
Diseases
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Auditory system disorder
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Inherited auditory system disease
/
Nonsyndromic genetic hearing loss
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Autosomal dominant nonsyndromic hearing loss
Hearing loss, autosomal dominant 37
rare
Identifiers
MONDO:0032802
OMIM:618533
Causal genes
COL11A1
Part of
Autosomal dominant nonsyndromic hearing loss
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