Autosomal recessive nonsyndromic hearing loss 42

MONDO:0012326

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ILDR1 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 42, DFNB42, ILDR1 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 42, autosomal recessive nonsyndromic deafness 42, autosomal recessive nonsyndromic deafness caused by mutation in ILDR1, autosomal recessive nonsyndromic deafness type 42, deafness, autosomal recessive 42

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 42 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 42 (0)

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