has material basis in germline mutation in CDC14A autosomal recessive nonsyndromic hearing loss 32 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/551 https://www.malacards.org/card/autosomal_recessive_nonsyndromic_deafness_32 https://www.malacards.org/card/deafness_autosomal_recessive_32_with_or_without_immotile_sperm autosomal recessive deafness 32 DFNB32 An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3. OMIM:608653 DOID:0110466 autosomal recessive nonsyndromic deafness 105 CDC14A autosomal recessive nonsyndromic deafness autosomal recessive nonsyndromic deafness caused by mutation in CDC14A autosomal recessive nonsyndromic deafness type 105 deafness, autosomal recessive 32, with or without immotile sperm GARD:0022610 MESH:C563884 deafness, autosomal recessive 32 autosomal recessive nonsyndromic deafness type 32 autosomal recessive deafness 105 deafness, autosomal recessive type 105 DOID:0110491 DFNB105 autosomal recessive nonsyndromic deafness 32 MEDGEN:373370 UMLS:C1837608 MONDO:0012091 deafness, autosomal recessive 105 hearing loss, autosomal recessive