Phenotypes for disease #05399 (DFNB32 (deafness, autosomal recessive, type 32 (DFNB-32)), OMIM:608653)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000207413 Non-syndromic hearing loss Non-syndromic hearing loss Congenital onset, severe-to-profound hearing loss Familial, autosomal recessive 43y - - - - Barbara Vona 00269609
0000207414 Non-syndromic hearing loss Non-syndromic hearing loss CDC14A has been recognized to cause hearing impairment and infertile male syndrome (HIIMS). We currently do not know the potential impact of the variant on the fertility of the two males in this family. Familial, autosomal recessive - - - - - Barbara Vona 00269610
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