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Autosomal recessive nonsyndromic hearing loss 36

rare

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ESPN gene.

Identifiers
MONDO:0012170 OMIM:609006
Causal genes
ESPN
Part of
Hearing loss, autosomal recessive
Also known as
deafness, neurosensory, without vestibular involvement, autosomal dominant

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