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Autosomal recessive nonsyndromic hearing loss 47

rare

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 2p25.1-p24.3.

Identifiers
MONDO:0012375 OMIM:609946
Part of
Hearing loss, autosomal recessive
Also known as
deafness, neurosensory, autosomal recessive 47

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