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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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Hearing loss, autosomal recessive
Hearing loss, autosomal recessive 106
rare
Identifiers
MONDO:0033198
OMIM:617637
Causal genes
EPS8L2
Part of
Hearing loss, autosomal recessive
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