All diseases

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00174 FH hypercholesterolemia, familial (FH) - AD 2962 2944 ABCA1, APOA2, EPHX2, GHR, ITIH4, LDLR, PPP1R17 - -
05708 FHCL1 hypercholesterolemia, familial, type 1 (FHCL1) 143890 AD 1 1 APOA2, EPHX2, GHR, LDLR - -
02489 GHIP hormomen, growth, insensitivity, partial (GHIP) 604271 AD - - GHR, GHSR - -
01008 IGHD1B growth hormone deficiency, isolated, type IB (IGHD-1B) 612781 - 21 - GH1, GHRHR - -
06761 IGHD4 Growth hormone deficiency, isolated, type IV 618157 AR - - GHRHR - -
02017 Laron Laron syndrome 262500 AR 46 46 GHR - -
Legend   How to query  


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