All diseases

8 entries on 1 page. Showing entries 1 - 8.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03275 ARCL1C cutis laxa, autosomal recessive, type IC (ARCL-1C) 613177 AR 10 9 LTBP4 - -
04565 DASS dental anomalies and short stature (DASS) 601216 AR - - LTBP3 - -
02331 GLC3B glaucoma, congenital, primary infantile, type 3B (GLC-3B) 600975 - 1 1 CYP1B1, LTBP2 - -
03246 GLC3D glaucoma, congenital, primary, type 3D (GLC-3D) 613086 - 21 19 LTBP2 - -
06120 GPHYSD3 Geleophysic dysplasia 3 617809 AD - - LTBP3 - -
01924 MSPKA microspherophakia and/or megalocornea, with ectopia lentis, with/without secondary glaucoma (MSPKA) 251750 AR 7 7 LTBP2 - -
03251 STHAG6 agenesis, tooth, selective, type 6 (STHAG-6) 613097 - - - LTBP3 - -
03734 WMS3 Weill-Marchesani syndrome, type 3 (WMS-3) 614819 AR 1 1 LTBP2 - -
Legend   How to query  


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