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
04389 DYT23 dystonia?, type 23 (DYT-23) 614860 - - - CACNA1B - -
06831 NEDNEH Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements 618497 AR - - CACNA1B - -
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