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
02309 DFNA4A deafness, autosomal dominant, type 4A (DFNA-4A) 600652 AD 1 1 MYH14 - -
03613 PNMHH neuropathy, peripheral, myopathy, hoarseness, and hearing loss (PNMHH) 614369 AD - - MYH14 - -
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