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
06481 CASGID ?Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development 618339 AD - - GLS - -
06480 EIEE71 Epileptic encephalopathy, early infantile, 71 618328 AR - - GLS - -
06484 GDPAG Global developmental delay, progressive ataxia, and elevated glutamine 618412 AR 1 - GLS - -
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