Autoimmune polyendocrinopathy type 1 (Q66125): Difference between revisions
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Poliendocrinopatia autoimune tipo 1 ou síndrome APECED é uma doença genética que se manifesta na infância ou início da adolescência com uma combinação de candidíase mucocutânea crônica, hipoparatireoidismo e falência adrenal autoimune. | |||
| description / en | description / en | ||
Autoimmune polyendocrinopathy type 1, or APECED syndrome, is a genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure. | |||
Revision as of 13:55, 14 August 2026
Autoimmune polyendocrinopathy type 1, or APECED syndrome, is a genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1646077225 |
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| English | Autoimmune polyendocrinopathy type 1 |
Autoimmune polyendocrinopathy type 1, or APECED syndrome, is a genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure. |
