All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01320 AAT4 aneurysm, aortic, thoracic, familial, type 4 (AAT4) 132900 - 2 - MYH11 - -
02309 DFNA4A deafness, autosomal dominant, type 4A (DFNA-4A) 600652 AD 1 1 MYH14 - -
07031 MMIHS megacystis-microcolon-intestinal hypoperistalsis syndrome, type 2 619351 AR - - MYH11 - -
03613 PNMHH neuropathy, peripheral, myopathy, hoarseness, and hearing loss (PNMHH) 614369 AD - - MYH14 - -
07032 VSCM2 myopathy, visceral, type 2 619350 AD - - MYH11 - -
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