All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06126 DFNB111 Deafness, autosomal recessive 111 618145 AR - - MPZL2 - -
05086 HL hearing loss (HL) - - 1295 1182 C10orf90, FAM179A, GRAP, MPZL2, PDZD7, PKHD1L1, USP48 - -
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