hemophagocytic syndrome
1hemophagocytic syndrome — see under lymphohistiocytosis …
2Hemophagocytic lymphohistiocytosis — A rare, cancer like disorder in which both histiocytes and lymphocytes start to proliferate and attack body tissues or organs. It can be an inherited condition, or it can occur as a result of immunosuppression (as in organ transplants) or… …
3Hemophagocytic lymphohistiocytosis — Infobox Disease Name = PAGENAME Caption = Light microscopic image of bone marrow showing stromal macrophages containing numerous red blood cells in their cytoplasm DiseasesDB = 31418 ICD10 = ICD10|D|76|1|d|70 ICD9 = ICD9|288.4 ICDO = OMIM =… …
4syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …
5macrophage activation syndrome — hemophagocytic lymphohistiocytosis …
6Hermansky–Pudlak syndrome — Classification and external resources ICD 10 E70.3 (ILDS E70.360) OMIM 203300 …
7Chédiak–Higashi syndrome — Classification and external resources ICD 10 E70.3 (E70.340 ILDS) ICD 9 288.2 …
8Cohen syndrome — Classification and external resources OMIM 216550 DiseasesDB 29622 Cohen syndrome (also known as Pepper syndrome or Cervenka syndrome, named afte …
9Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome — Classification and external resources OMIM 609528 Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome (also known as CEDNIK syndrome ) is a cutaneous condition caused by mutation in the SNAP29 gene.[ …
10Macrophage-activation syndrome — (MAS) is a severe, potentially life threatening, complication of several chronic rheumatic diseases of childhood. It occurs most commonly with systemic onset juvenile idiopathic arthritis (SoJIA), which is also known as Still s disease. In… …
