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autoimmune polyendocrinopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0017278

A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues. [ NCIT:C129726 ]

Synonyms: Antiphospholipid Syndrome autoimmune polyglandular syndrome autoimmune polyendocrine syndrome APS autoimmune polyendocrine syndrome; polyglandular autoimmune syndrome Lloyd's syndrome autoimmune polyendocrinopathy syndrome autoimmune polyglandular syndrome(s) autoimmune polyendocrinopathy autoimmune polyglandular failure

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C84576 (MONDO:equivalentTo)
  • DOID:14040 (MONDO:equivalentTo)
  • NANDO:2100125 (https://orcid.org/0000-0003-0011-764X)
  • SCTID:41864002 (MONDO:equivalentTo)
  • UMLS:C0085409 (MONDO:equivalentTo)
  • NCIT:C129726 (MONDO:equivalentTo)
  • icd11.foundation:548357900 (Orphanet:282196)
  • ICD10CM:E31.0 (Orphanet:282196/ntbt)
  • ICD9:258.8 (MONDO:relatedTo)
  • MEDGEN:39042 (MONDO:equivalentTo)
  • Orphanet:282196 (MONDO:equivalentTo)
  • NORD:790 (MONDO:NORD)
  • GARD:21116 (MONDO:GARD)
Subsets

gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders

exactMatch

http://identifiers.org/snomedct/41864002

http://purl.obolibrary.org/obo/DOID_14040

http://purl.obolibrary.org/obo/NCIT_C84576

http://linkedlifedata.com/resource/umls/id/C0085409

http://purl.obolibrary.org/obo/NCIT_C129726

http://purl.bioontology.org/ontology/ICD10CM/E31.0

http://identifiers.org/medgen/39042

http://www.orpha.net/ORDO/Orphanet_282196

id

MONDO:0017278