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
04612 HPMRS5;GPIBD11 hyperphosphatasia with mental retardation syndrome, type 5 (HPMRS-5, glycosylphosphatidylinositol deficiency, type 11 (GPIBD-11)) 616025 AR - - PIGW - autosomal recessive
Legend   How to query  


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