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
05928 SCN neutropenia, severe congenital (SCN) - - 26 26 SRP54 - -
05929 SCN8 neutropenia, severe congenital, type 8, autosomal dominant (SCN8) 618752 AD - - SRP54 - -
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