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
00668 KLEFS Kleefstra syndrome (KLEFS) - - 32 30 EHMT1, MLL3 - -
05770 KLEFS2 Kleefstra syndrome, type 2 (KLEFS2) 617768 AD 5 4 MLL3 - developmental delay, intellectual disability, behavioral and psychiatric problems, hypotonia, seizures, short stature
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