All diseases

11 entries on 1 page. Showing entries 1 - 11.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01890 - growth hormone insensitivity with immunodeficiency 245590 - 8 8 STAT5B - -
04678 ADMIO1 autoimmune disease, multisystem, infantile-onset 615952 AD 2 2 STAT3 - -
01398 HIES1 Hyper-IgE recurrent infection syndrome 147060 AD 14 14 STAT3 - -
00139 ID intellectual disability (ID) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
04677 IMD31A immunodeficiency, type 31A, mycobacteriosis, autosomal dominant (IMD-31A) 614892 AD 8 8 STAT1 - -
03438 IMD31B immunodeficiency, type 31B, mycobacterial and viral infections, autosomal recessive (IMD-31B) 613796 AR 8 8 STAT1 - -
03566 IMD31C;CANDF7 immunodeficiency, type 31C, autosomal dominant (IMD-31C, candidiasis, familial, type 7 (CANDF-7)) 614162 AD 92 92 STAT1 - -
06165 IMD44 Immunodeficiency 44 616636 AR - - STAT2 - -
04679 PML leukemia, acute promyelocytic, somatic (PML) 102578 - - - STAT5B - -
03107 SLEB11 lupus erythematosus, systemic, type 11 (SLEB-11) 612253 - - - STAT4 - -
02111 TYRSN2 tyrosinemia, type II 276600 AR - - TAT - -
Legend   How to query  


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