has material basis in germline mutation in AIRE adrenal gland disorder autoimmune polyendocrine syndrome type 1 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/autoimmune_polyendocrine_syndrome_type_1 https://www.malacards.org/card/autoimmune_polyendocrine_syndrome_type_i_with_or_without_reversible_metaphyseal_dysplasia SCTID:11244009 AIRE autoimmune polyendocrinopathy APS type 1 autoimmune polyendocrine syndrome type 1 autoimmune hypoparathyroidism-chronic candidiasis-Addison disease syndrome Autoimmune Polyglandular Syndrome Type 1 autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy DOID:0050167 autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) 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. ICD9:258.8 APS1 autoimmune polyendocrinopathy syndrome type 1 aire autoimmune polyendocrinopathy hypoparathyroidism-Addison disease-mucocutaneous candidiasis syndrome Whitaker syndrom autoimmune polyendocrinopathy caused by mutation in aire NANDO:2200738 NCIT:C129727 autoimmune polyendocrine syndrome, type I, with or without reversible metaphyseal dysplasia autoimmune polyendocrinopathy caused by mutation in AIRE OMIM:240300 ham syndrome autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia autoimmune polyglandular syndrome type 1 NANDO:2200346 GARD:0008466 polyglandular autoimmune syndrome type 1 NORD:798 APECED syndrome multiple endocrine deficiency-Addison disease-candidiasis syndrome MEDAC syndrome Orphanet:3453 MEDGEN:39125 MONDO:0009411 Whitaker syndrome UMLS:C0085859 autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome obsolete acquired chronic primary adrenal insufficiency hereditary hypoparathyroidism autoimmune polyendocrinopathy autoimmune hypoparathyroidism acquired primary ovarian failure