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| Term | autoimmune polyendocrine syndrome type 1 | ID (Ontology) | DOID:0050167 (Human Disease) |
| 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." [url:https\://rarediseases.info.nih.gov/diseases/8466/autoimmune-polyglandular-syndrome-type-1] {comment="sn:IEDB"} | ||
| Also Known As | "autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy" ; "Autoimmune Polyglandular Syndrome I" ; "Whitaker syndrome" | ||
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autoimmune disease of endocrine system |__autoimmune polyendocrine syndrome |__autoimmune polyendocrine syndrome type 1 |
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| Is a | autoimmune polyendocrine syndrome | ||
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GARD:8466 MIM:240300 |
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