Autosomal recessive nonsyndromic hearing loss 67

MONDO:0012460

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LHFPL5 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 67, DFNB67, LHFPL5 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 67, autosomal recessive nonsyndromic deafness 67, autosomal recessive nonsyndromic deafness caused by mutation in LHFPL5, autosomal recessive nonsyndromic deafness type 67, deafness, autosomal recessive 67

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 67 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 67 (0)

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