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Autosomal recessive nonsyndromic hearing loss 103

MONDO:0014469

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CLIC5 gene.

Also known as: CLIC5 autosomal recessive nonsyndromic deafness, DFNB103, autosomal recessive deafness 103, autosomal recessive nonsyndromic deafness 103, autosomal recessive nonsyndromic deafness caused by mutation in CLIC5, autosomal recessive nonsyndromic deafness type 103, deafness, autosomal recessive 103, deafness, autosomal recessive type 103

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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