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Autosomal recessive nonsyndromic hearing loss 15

MONDO:0011160

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GIPC3 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 15, DFNB15, DFNB72, DFNB95, GIPC3 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 15, autosomal recessive deafness 72, autosomal recessive deafness 95

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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