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
01959 CMYO4A;CFTD myopathy, congenital, type 4A 255310 AD 56 53 TPM3 - -
02840 CMYO4B myopathy, congenital, type 4B 609284 AR 1 1 TPM3 - -
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