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
01353 GPS Gray platelet syndrome 139090 AR - - NBEAL2 - -
07073 NEDEGE neurodevelopmental disorder with or without early-onset generalized epilepsy 619157 AD 1 1 NBEA - -
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