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immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome (DOID:0090110)
Alliance: disease page
Synonyms: Autoimmune enteropathy type 1; autoimmunity-immunodeficiency syndrome, X-linked; diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea; diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked; DMSD; IDDM-secretory diarrhea syndrome; immunodeficiency, polyendocrinopathy, and enteropathy, X-linked; immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked; IPEX; X-linked autoimmunity-allergic dysregulation syndrome; XLAAD; XPID
Alt IDs: OMIM:304790, ICD10CM:E31.0, ORDO:37042
Definition: An autoimmune hypersensitivity disease that is characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has material_basis_in X-linked recessive mutation in the forkhead box P3 (FOXP3) gene on chromosome Xp11.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory