All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00244 MYOP myopathy (MYOP) - - 947 878 FDX1L, FXR1, JPH1, MLIP, MYL1, NDUFAF7, PLIN4 - -
06601 MYOPMIL ?Myopathy, congenital proximal, with minicore lesions 618823 AR - - FXR1 - -
06600 MYORIBF ?Myopathy, congenital, with respiratory insufficiency and bone fractures 618822 AR - - FXR1 - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.