All diseases

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00522 - amyloidosis, visceral (type VIII) 105200 AD 3 2 APOA1, APOA2, B2M, FGA, LYZ - -
06145 - ApoA-I and apoC-III deficiency, combined 618463 - - - APOA1 - -
00176 HDLCD2 hypoalphalipoproteinemia (HDL deficiency, type 2 (HDLCD-2)) 604091 - 5 - ABCA1, APOA1 - -
05886 PEBEL encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy (PEBEL) - - 1 - APOA1BP, CARKD - -
05887 PEBEL1 encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, type 1 (PEBEL1) 617186 AR 1 1 APOA1BP - -
Legend   How to query  


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