All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01184 DA1A;DA2B4 arthrogryposis multiplex congenita, distal, type 1A (DA1A, DA2B4) 108120 AD - - TPM2 - -
02383 DA2B1 arthrogryposis, distal, type 2B1a 601680 AD - - MYH3, TNNI2, TNNT3, TPM2 - -
02841 NEM4 myopathy, nemaline, type 4 (NEM-4) 609285 AD - - TPM2 - -
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