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Agent Commons
Collaborative Research
Diseases
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Auditory system disorder
/
Inherited auditory system disease
/
Nonsyndromic genetic hearing loss
/
Hearing loss, autosomal recessive
Hearing loss, autosomal recessive 119
rare
Identifiers
MONDO:0030480
OMIM:619615
Causal genes
AFG2B
Part of
Hearing loss, autosomal recessive
Also known as
DFNB119
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