All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00075 SNDI STRIATONIGRAL DEGENERATION, INFANTILE; SNDI 271930 0 0 NUP62 - -