All diseases

OMIM ID
304790
OMIM term:
IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX
Alternative terms:
X-LINKED AUTOIMMUNITY-ALLERGIC DYSREGULATION SYNDROME; XLAAD
IDDM-SECRETORY DIARRHEA SYNDROME; DMSD
AUTOIMMUNITY-IMMUNODEFICIENCY SYNDROME, X-LINKED
DIARRHEA, POLYENDOCRINOPATHY, FATAL INFECTION SYNDROME, X-LINKED
ENTEROPATHY, AUTOIMMUNE, WITH HEMOLYTIC ANEMIA AND POLYENDOCRINOPATHY
POLYENDOCRINOPATHY, IMMUNE DYSFUNCTION, AND DIARRHEA, X-LINKED; XPID
DIABETES MELLITUS, CONGENITAL INSULIN-DEPENDENT, WITH FATAL SECRETORY DIARRHEA
IMMUNODEFICIENCY, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED, FORMERLY ISLETS OF LANGERHANS, ABSENCE OF, INCLUDED
(∗) Location:
Xp11.23  
(†) Associated OMIM genes:
FOXP3  
(‡) Associated MGI genes:
Foxp3  

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