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
00179 BDB1 brachydactyly, type B1 (BDB1) 113000 AD 12 12 ROR2 - -
00139 ID intellectual disability (ID) - - 2794 2475 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 556 more - -
00180 RRS Robinow syndrome, autosomal recessive (RRS) - AD 99 98 NXN, ROR2 - -
05842 RRS1 Robinow, autosomal recessive syndrome, type 1 (RRS1) 268310 AR 2 1 ROR2 - -
Legend   How to query  


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