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
03943 DFNB88 deafness, autosomal recessive, type 88 (DFNB-88) 615429 AR - - ELMOD3 - -
04562 NEM10 myopathy, nemaline, type 10 (NEM-10) 616165 AR 1 1 LMOD3 - -
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