All diseases

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00750 ALGS syndrome, Alagille (ALGS) 118450 - 1002 383 JAG1, NOTCH2 - autosomal dominant
01027 DCHE deafness, congenital heart defects, posterior embryotoxon (DCHE) 617992 - 1 1 JAG1 - -
00139 ID intellectual disability (ID) - - 1846 1579 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 536 more - -
00389 TOF tetralogy of Fallot (TOF) 187500 - 101 93 GATA4, GATA6, GDF1, JAG1, NKX2-5, TBX1, ZFPM2 - -
Legend   How to query