has material basis in germline mutation in PJVK autosomal recessive nonsyndromic hearing loss 59 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/551 https://www.malacards.org/card/deafness_autosomal_recessive_59 DFNB59 GARD:0022622 DOID:0110511 PJVK autosomal recessive nonsyndromic deafness MESH:C565698 autosomal recessive deafness 59 Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PJVK gene. autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness type 59 OMIM:610220 deafness, autosomal recessive 59 MEDGEN:387899 UMLS:C1857744 deafness, autosomal recessive type 59 autosomal recessive nonsyndromic deafness caused by mutation in PJVK autosomal recessive nonsyndromic hearing loss 59 MONDO:0012445 hearing loss, autosomal recessive