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
06243 IDDSFTA Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities 618092 AD 6 6 BCL11B - -
06234 IMD49 immunodeficiency, type 49 617237 AD - - BCL11B - -
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