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
01218 - Burkitt lymphoma 113970 - 63 63 MYC - -
00870 FGLDS1 Feingold syndrome, type 1 164280 AD 4 4 MYCN - esophageal atresias, duodenal atresias, microcephaly, learning disability, syndactyly, cardiac defect
00139 ID intellectual disability (ID) - - 2800 2481 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 556 more - -
07247 MPAPA megalencephaly-polydactyly syndrome 620748 AD - - MYCN - -
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