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
01398 - Hyperimmunoglobulin E syndrome 147060 - - - STAT3 - -
01676 - Disseminated atypical mycobacterial infection 209950 - - - IFNGR1, IFNGR2, IL12RB1, STAT1 - -
01890 - growth hormone insensitivity with immunodeficiency 245590 - - - STAT5B - -
02111 - Tyrosinemia type 2 276600 - - - TAT - -
03438 - Mycobacterial and viral infections, susceptibility to, autosomal recessive 613796 - - - STAT1 - -
04678 ADMIO autoimmune disease, multisystem, infantile-onset (ADMIO) 615952 - - - STAT3 - -
03566 CANDF-7 candidiasis, familial, type 7 (CANDF-7) 614162 - - - STAT1 - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
04677 IMD-31A immunodeficiency, type 31A, mycobacteriosis, autosomal dominant (IMD-31A) 614892 - - - STAT1 - -
04679 PML leukemia, acute promyelocytic, somatic (PML) 102578 - - - STAT5B - -
03107 SLEB-11 lupus erythematosus, systemic, type 11 (SLEB-11) 612253 - - - STAT4 - -
Legend   How to query