Hearing loss, X-linked 4
MONDO:0010238Any X-linked nonsyndromic deafness in which the cause of the disease is a mutation in the SMPX gene.
Also known as: SMPX X-linked nonsyndromic deafness, X-linked nonsyndromic deafness caused by mutation in SMPX, deafness, X-linked 4, deafness, X-linked 4, X-linked dominant, deafness, X-linked type 4, deafness, nonsyndromic sensorineural progressive 6, DFNX4, deafness, X-linked 6, progressive
60 clinical trials for this condition and its sub-types.
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