All diseases

1 entry on 1 page. Showing entry 1.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05402 HPMRS6;GPIBD12 hyperphosphatasia with mental retardation syndrome, type 6 (HPMRS-6, glycosylphosphatidylinositol deficiency, type 12 (GPIBD-12)) 616809 AR 1 - PIGY - autosomal recessive
Legend   How to query  


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