All diseases

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06732 SHFM1 Split-hand/foot malformation 1 183600 - - - DLX5 - -
01746 SHFM1D split-hand/foot malformation, type 1 with sensorineural hearing loss (SHFM-1D) 220600 AR - - DLX5 - -
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.