All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00108 DYT dystonia (DYT) - - 175 215 GNAL, KMT2B, THAP1 - -
05849 DYT28 dystonia, type 28, childhood-onset (DYT28) 617284 AD 2 1 KMT2B - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
07146 MRD68 intellectual developmental disorder, autosomal dominant, type 68 619934 AD - - KMT2B - -
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