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DOID:0050167 - autoimmune polyendocrine syndrome type 1
Disease Ontology Definition:An autoimmune polyendocrine syndrome that is inherited in an autosomal recessive fashion, which is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs.
Synonyms: Autoimmune Polyglandular Syndrome I, Whitaker syndrom, autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:240300 - autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia; aps1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autoimmune polyendocrine syndrome (is_a)