All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05555 NEDIDHA neurodevelopmental disorder, impaired intellectual development, hypotonia, and ataxia (NEDIDHA) 618292 AR 10 10 DOCK3 - autosomal recessive
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