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
01469 - neutrophilia, hereditary 162830 - - - CSF3R - -
06009 SCN7 Neutropenia, severe congenital, 7, autosomal recessive 617014 AR - - CSF3R - -
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