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Autosomal recessive nonsyndromic hearing loss 18B

MONDO:0013985

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

Also known as: autosomal recessive nonsyndromic hearing loss 18B, DFNB18B, OTOG autosomal recessive nonsyndromic deafness, autosomal recessive deafness 18B, autosomal recessive nonsyndromic deafness 18B, autosomal recessive nonsyndromic deafness caused by mutation in OTOG, autosomal recessive nonsyndromic deafness type 18B, deafness, autosomal recessive 18B

60 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hearing loss disorder (254) Nervous system disorder (217) Hereditary disease (172) Perceptual disorders (21) Hearing disorder (19) Human disease (14) Hereditary neurological disease (5) Autosomal recessive disease (4) Nonsyndromic genetic hearing loss (3)
Trials to join now! 21 Not yet recruiting 13 Not yet finished but already full! 8 Completed 17 Terminated 1
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