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
00139 ID intellectual disability (ID) - - 2694 2376 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
05262 SGBS Simpson-Golabi-Behmel syndrome (SGBS) - - 59 59 GPC3 - -
00773 SGBS1 Simpson-Golabi-Behmel syndrome, type 1 (SGBS1) 312870 XLR 1 1 GPC3 - -
00774 WT1 Wilms tumor, type 1, somatic (WT-1, nephroblastoma) 194070 AD;SMu 7 7 BRCA2, GPC3, H19, WT1 - -
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