Carrion's Disease malady
Categories: Infectious diseases, Rare diseases, Cardiovascular diseases
Aliases & Descriptions for Carrion's Disease:
Global: Infectious diseases, Rare diseases
Anatomical: Cardiovascular diseases
ICD10: 29 28
Rare infectious diseases
Disease Ontology:11 A bartonellosis that results in infection located in endothelial cells or located in red blood cells, has material basis in bartonella bacilliformis, which is transmitted by sandflies of genus lutzomyia. the infection has acute and chronic phases. the acute phase is characterized by severe hemolytic anemia and transient immunosuppression. the chronic phase is characterized by verruga peruana lesions which may ulcerate and bleed.
MalaCards based summary: Carrion's Disease, also known as oroya fever, is related to cat-scratch disease and ornithosis. An important gene associated with Carrion's Disease is ASXL3 (Additional Sex Combs Like 3, Transcriptional Regulator), and among its related pathways is Malaria. Affiliated tissues include endothelial cells or, endothelial and liver.
CDC:2 Bartonella bacteria cause several diseases in humans. The three most common are cat scratch disease, caused by B. henselae; trench fever, caused by B. quintana; and Carrión's disease, caused by B. bacilliformis.
Drugs for Carrion's Disease (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):(show top 50) (show all 73)
Interventional clinical trials:(show all 32)
Search NIH Clinical Center for Carrion's Disease
MalaCards organs/tissues related to Carrion's Disease:34
Endothelial, Liver, Breast, Myeloid
FMA organs/tissues related to Carrion's Disease:17
Endothelial cells or
Articles related to Carrion's Disease:(show all 18)
Search GEO for disease gene expression data for Carrion's Disease.
Cellular components related to Carrion's Disease according to GeneCards Suite gene sharing:
Biological processes related to Carrion's Disease according to GeneCards Suite gene sharing:(show all 7)
29ICD10 via Orphanet
38MESH via Orphanet
51OMIM via Orphanet
61SNOMED-CT via Orphanet
65Tumor Gene Family of Databases
67UMLS via Orphanet