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 CFTD myopathy, congenital, with fiber type disproportion (CFTD) 255310 - 53 52 ACTA1, MYH7, RYR1, SEPN1, TPM2, TPM3 - -
02840 NEM-1 myopathy, nemaline, type 1 (NEM-1) 609284 - 0 0 TPM3 - -
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