Medical dictionary. 2011.
familial hemophagocytic reticulosis — familial histiocytic reticulosis familial hemophagocytic lymphohistiocytosis … Medical dictionary
Hemophagocytic 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 =… … Wikipedia
Hemophagocytic 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… … Medical dictionary
lymphohistiocytosis — Proliferation or infiltration of lymphocytes and histiocytes. familial erythrophagocytic l. (FEL) SYN: familial hemophagocytic l.. familial hemophagocytic l. (FMLH) an extremely rare, usually fatal disease of childhood characterized by multiorgan … Medical dictionary
STX11 — Syntaxin 11, also known as STX11, is a human gene.cite web | title = Entrez Gene: STX11 syntaxin 11| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=8676| accessdate = ] ee also* Hemophagocytic… … Wikipedia
Perforin — 1 (pore forming protein), also known as PRF1, is a human gene.cite web | title = Entrez Gene: PRF1 perforin 1 (pore forming protein)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5551| accessdate = ]… … Wikipedia
X-linked lymphoproliferative disease — Classification and external resources ICD 10 D82.3 OMIM 308240 300635 … Wikipedia
MACPF — Pfam box Symbol = MACPF Name = MAC/Perforin domain width = caption = Pfam= PF01823 InterPro= IPR001862 SMART= MACPF PROSITE = PDOC00251 SCOP = TCDB = 1.C.39 OPM family= OPM protein= PDB=The MACPF protein superfamily is named after a domain that… … Wikipedia
Primary immunodeficiency — Primary immunodeficiencies are disorders in which part of the body s immune system is missing or does not function properly. To be considered a primary immunodeficiency, the cause of the immune deficiency must not be secondary in nature (i.e.,… … Wikipedia
GNLY — Granulysin, also known as GNLY, is a human gene.cite web | title = Entrez Gene: GNLY granulysin| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=10578| accessdate = ] PBB Summary section title = summary text … Wikipedia
