A disorder caused by the presence of autoantibodies directed against phospholipids, causing a hypercoaguable state, which may result in blood clots, stroke, heart attack, and in women, significant pregnancy-related complications, including miscarriage and still birth. The syndrome is often associated with other autoimmune disorders, most commonly lupus erythematosus, and infections, including syphilis and Lyme disease. [ NCIT:C61283 ]
Synonyms: familial lupus anticoagulant antiphospholipid syndrome Hughes syndrome antiphospholipid antibody syndrome
Term information
- MEDGEN:38834 (MONDO:equivalentTo)
- MESH:D016736 (MONDO:equivalentTo)
- DOID:2988 (MONDO:equivalentTo)
- ICD10CM:D68.61 (MONDO:equivalentTo)
- Orphanet:80 (OMIM:107320)
- EFO:0002689 (MONDO:equivalentTo)
- UMLS:C0085278 (MONDO:equivalentTo)
- ICD9:279.49 (MONDO:relatedTo)
- GARD:5824 (MONDO:GARD)
- NCIT:C61283 (MONDO:equivalentTo)
- icd11.foundation:1173370808 (Orphanet:80)
- SCTID:26843008 (MONDO:equivalentTo)
gard_rare, ordo_disorder, otar, rare, orphanet_rare
http://purl.obolibrary.org/obo/NCIT_C61283
http://identifiers.org/snomedct/26843008
http://linkedlifedata.com/resource/umls/id/C0085278
http://identifiers.org/medgen/38834
http://purl.obolibrary.org/obo/DOID_2988
http://identifiers.org/mesh/D016736
http://purl.bioontology.org/ontology/ICD10CM/D68.61
http://www.orpha.net/ORDO/Orphanet_80