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
01597 CPVT tachycardia, ventricular (CPVT) 192605 AD 13 13 GNAI2, TECRL - -
05143 CPVT3 tachycardia, ventricular, catecholaminergic polymorphic, type 3 614021 AR - - TECRL - -
00139 ID intellectual disability (ID) - - 2792 2473 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 556 more - -
00813 MRT14 mental retardation, autosomal recessive, type 14 (MRT-14) 614020 AR - - TECR - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.