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
05962 NEDAUS neurodevelopmental disorder with/without autism or seizures 619239 AD 2 2 CUL3 - -
03669 PHA2E pseudohypoaldosteronism type 2E (PHA2E) 614496 AD - - CUL3 - -
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