All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
07229 CHOCNS Chilton-Okur-Chung neurodevelopmental syndrome 619841 AD - - CDC42BPB - developmental delay (12/13), intellectual disability (7/13), hypotonia (8/11), autism spectrum disorder (8/12)
05772 HLH lymphohistiocytosis, hemophagocytic - IC 4 4 CDC42 - -
05221 TKS Takenouchi-Kosaki syndrome (TKS) 616737 AD 6 6 CDC42 - -
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