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Autosomal recessive nonsyndromic hearing loss 5

MONDO:0000912

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 14q12.

Also known as: DFNB5, autosomal recessive deafness 5, autosomal recessive nonsyndromic deafness 5, autosomal recessive nonsyndromic deafness type 5, deafness, autosomal recessive 5, neurosensory nonsyndromic recessive deafness 5

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Hearing loss disorder (284) Nervous system disorder (231) Hereditary disease (176) Hearing disorder (24) Perceptual disorders (22) Human disease (14) Hereditary neurological disease (6) Autosomal recessive disease (4) Nonsyndromic genetic hearing loss (4)
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  • Newborn screening study aims to catch rare diseases at birth

    Diagnosis Ongoing

    This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

    Sponsor: RTI International • Aim: Diagnosis

    Last updated Jul 03, 2026 00:00 UTC

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