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Hearing loss, autosomal recessive 118, with cochlear aplasia

MONDO:0030449

Also known as: DFNB118, deafness, autosomal recessive 118, with cochlear aplasia

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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  • Brain implant offers sound hope for deaf children born without ears

    Disease control Completed

    This study tested a special hearing device called an auditory brainstem implant in 10 children aged 2 to 5 who are profoundly deaf due to missing or damaged inner ear parts. Unlike a cochlear implant, this device is placed directly on the brainstem during surgery. The main goal w…

    Phase: PHASE1 • Sponsor: Laurie Eisenberg • Aim: Disease control

    Last updated Jun 26, 2026 17:22 UTC

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