All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01710 GRBGD Greenberg skeletal dysplasia 215140 AR 1 1 LBR - -
01495 PHA Pelger-Huet anomaly (PHA) 169400 AD - - LBR - -
06033 PHASK Pelger-Huet anomaly with mild skeletal anomalies 618019 - - - LBR - -
03341 Reynolds Reynolds syndrome 613471 AD - - LBR - -
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