acquired purpura fulminans
A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. PF may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of PF that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic PF. [ Orphanet:49566 ]
Term info
- UMLS:C0043068 (Orphanet:49566/e)
- MedDRA:10037556 (Orphanet:49566/e)
- SCTID:725157006 (MONDO:equivalentTo)
- UMLS:CN205163 (MONDO:equivalentTo)
- MESH:D014884 (Orphanet:49566/e)
- Orphanet:49566 (MONDO:equivalentTo)
- MESH:D055665 (Orphanet:49566/e)
- UMLS:C4510896 (MONDO:equivalentTo)
ordo_disease
http://identifiers.org/meddra/10037556
A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. PF may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of PF that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic PF.
http://purl.obolibrary.org/obo/Orphanet_49566, http://linkedlifedata.com/resource/umls/id/C4510896, http://identifiers.org/snomedct/725157006, http://linkedlifedata.com/resource/umls/id/CN205163
acquired purpura fulminans, acquired PF
MONDO:0018854