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
01841 - anemia, hemolytic, due to hexokinase deficiency 235700 AR - - HK1 - -
02539 HMSNR;CMT4G neuropathy, hereditary motor and sensory, Russe type (CMT4G) 605285 AR 1 1 HK1 - autosomal recessive
05727 NEDVIBA neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA) 618547 AD 7 7 HK1 - -
05724 RP79 retinitis pigmentosa, type 79 (RP79) 617460 AD - - HK1 - -
Legend   How to query  


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