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
01468 neutropenia neutropenia, cyclical 162800 AD - - ELANE - -
01636 SCN1 neutropenia, congenital, severe, autosomal dominant (SCN1) 202700 AD - - ELANE - -
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