MCID: ACQ039
MIFTS: 18
|
Acquired Purpura Fulminans
Categories:
Blood diseases, Rare diseases, Skin diseases
|
|
|
MalaCards integrated aliases for Acquired Purpura Fulminans:
Name: Acquired Purpura Fulminans
58
Characteristics:Classifications:
ICD10:
32
Orphanet: 58
![]() |
Orphanet: 58 A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. It may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of the disorder that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic purpura fulminans. MalaCards based summary: Acquired Purpura Fulminans is related to purpura fulminans and purpura. Affiliated tissues include skin, and related phenotypes are acrocyanosis and thrombocytopenia |
Diseases in the Purpura Fulminans family:
Diseases related to Acquired Purpura Fulminans via text searches within MalaCards or GeneCards Suite gene sharing:
Graphical network of the top 20 diseases related to Acquired Purpura Fulminans:![]() |
Human phenotypes related to Acquired Purpura Fulminans:58 30 (show all 26)
|
|
Organs/tissues related to Acquired Purpura Fulminans:
MalaCards :
Skin
|
Articles related to Acquired Purpura Fulminans:
|
|
Search
GEO
for disease gene expression data for Acquired Purpura Fulminans.
|
|
|