Difference between revisions of "Template:Diseases of RBCs and megakaryocytes"
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| + | {{Navbox | ||
| + | | name = Diseases of RBCs and megakaryocytes | ||
| + | | title = [[Pathology]]: [[hematology]]{{·}} [[hematologic disease]]s of [[Red blood cell|RBC]]s and [[megakaryocyte]]s / [[Megakaryocyte-erythroid progenitor cell|MEP]] ([[ICD-10_Chapter_II:_Neoplasms%3B_Chapter_III:_Diseases_of_the_blood_and_blood-forming_organs%2C_and_certain_disorders_involving_the_immune_mechanism#D50-D89_-_Diseases_of_the_blood_and_blood-forming_organs_and_certain_disorders_involving_the_immune_mechanism|D50-69,74]], [[List of ICD-9 codes 280-289: Diseases of the blood and blood-forming organs|280-287]]) | ||
| + | | titlestyle = background:Silver | ||
| + | | groupstyle = background:MistyRose; | ||
| + | | belowstyle = background:MistyRose; | ||
| + | | group1 = [[Red blood cell|Red<br/>blood cells]] | ||
| + | | list1 = {{Navbox subgroup | ||
| + | | groupstyle = background-color: MistyRose; | ||
| + | |||
| + | | group1 = ↑ | ||
| + | | list1 = {{Navbox subgroup | ||
| + | | groupstyle = background-color:MistyRose;width:10em; | ||
| + | |liststyle = width:auto; | ||
| + | | group1 = [[Polycythemia]] | ||
| + | | list1 = [[Polycythemia vera]] | ||
| + | }} | ||
| + | |||
| + | | group2 = ↓ | ||
| + | | list2 = {{Navbox subgroup | ||
| + | | groupstyle = background-color:MistyRose;width:10em; | ||
| + | |liststyle = width:auto; | ||
| + | | group1 = [[Anemia]] | ||
| + | | list1 = {{Navbox subgroup | ||
| + | | groupstyle = background-color:MistyRose; | ||
| + | |||
| + | | group1 = [[Nutritional anemia|Nutritional]] | ||
| + | | list1 = [[Microcytic anemia|Micro-]]: [[Iron deficiency anemia]] ([[Plummer-Vinson syndrome]])<BR> | ||
| + | |||
| + | [[Macrocytic anemia|Macro-]]: [[Megaloblastic anemia]] ([[Pernicious anemia]]) | ||
| + | |||
| + | | group2 = [[Hemolytic anemia|Hemolytic]]<BR>(mostly [[Normocytic anemia|Normo-]]) | ||
| + | | list2 = {{Navbox subgroup | ||
| + | | groupstyle = background-color: MistyRose | ||
| + | |||
| + | | group1 = [[Congenital hemolytic anemia|Hereditary]] | ||
| + | | list1 = ''[[enzymopathy]]:'' [[Glucose-6-phosphate dehydrogenase deficiency|G6PD]]{{·}} ''[[glycolysis]]'' ([[Pyruvate kinase deficiency|PK]], [[Triosephosphate isomerase deficiency|TI]], [[Hexokinase deficiency|HK]]) | ||
| + | |||
| + | ''[[hemoglobinopathy]]:'' [[Thalassemia]] ([[alpha-thalassemia|alpha]], [[beta-thalassemia|beta]], [[delta-thalassemia|delta]]) {{·}} [[Sickle-cell disease]]/[[Sickle cell trait|trait]]{{·}} [[Hereditary persistence of fetal hemoglobin|HPFH]] | ||
| + | |||
| + | ''[[Red_blood_cell#Membranes_and_surface_proteins|membrane]]:'' [[Hereditary spherocytosis|Hereditary spherocytosis]] ([[Minkowski-Chauffard syndrome]]){{·}} [[Hereditary elliptocytosis|Hereditary elliptocytosis]] ([[Southeast Asian ovalocytosis]]){{·}} [[Hereditary stomatocytosis]] | ||
| + | |||
| + | | group2 =[[Acquired hemolytic anemia|Acquired]] | ||
| + | | list2 = [[Autoimmune hemolytic anemia|Autoimmune]] ([[Warm autoimmune hemolytic anemia|WAHA]], [[Cold agglutinin disease|CAD]], [[Paroxysmal cold hemoglobinuria|PCH]])<BR> | ||
| + | |||
| + | ''[[Red_blood_cell#Membranes_and_surface_proteins|membrane]]'' ([[Paroxysmal nocturnal hemoglobinuria|PNH]]) | ||
| + | |||
| + | [[Microangiopathic hemolytic anemia|MAHA]]{{·}} [[Thrombotic microangiopathy|TM]] ([[Hemolytic-uremic syndrome|HUS]]) | ||
| + | |||
| + | [[Drug-induced autoimmune hemolytic anemia|Drug-induced autoimmune]]{{·}}[[Drug-induced nonautoimmune hemolytic anemia|Drug-induced nonautoimmune]] | ||
| + | |||
| + | [[Hemolytic disease of the newborn]] | ||
| + | }} | ||
| + | |||
| + | | group3 = [[Aplastic anemia|Aplastic]]<BR>(mostly [[Normocytic anemia|Normo-]]) | ||
| + | | list3 = [[Congenital hypoplastic anemia|Hereditary]]: [[Fanconi anemia]]{{·}} [[Diamond–Blackfan anemia]]<BR> | ||
| + | |||
| + | Acquired: [[pure red cell aplasia|PRCA]]{{·}} [[Sideroblastic anemia]]{{·}} [[Myelophthisic anemia|Myelophthisic]] | ||
| + | |||
| + | | group4 = [[Red blood cell indices|Blood tests]] | ||
| + | | list4 = ''[[Mean corpuscular volume|MCV]]'' ([[Normocytic anemia|Normocytic]], [[Microcytic anemia|Microcytic]], [[Macrocytic anemia|Macrocytic]]){{·}} ''[[Mean corpuscular hemoglobin concentration|MCHC]]'' ([[Normochromic anemia|Normochromic]], [[Hypochromic anemia|Hypochromic]]) | ||
| + | |||
| + | }} | ||
| + | |||
| + | | group2 = Other | ||
| + | | list2 = [[Methemoglobinemia]]{{·}} [[Sulfhemoglobinemia]]{{·}} [[Reticulocytopenia]] | ||
| + | |||
| + | }} | ||
| + | }} | ||
| + | |||
| + | | group2 = [[Coagulation]]/<BR>[[coagulopathy]]/<BR>[[bleeding diathesis|bleeding<br/>diathesis]] | ||
| + | | list2 = {{Navbox subgroup | ||
| + | | groupstyle = background-color: MistyRose; | ||
| + | |||
| + | | group1 = ↑ | ||
| + | | list1 = {{Navbox subgroup | ||
| + | | groupstyle = background-color: MistyRose | ||
| + | |||
| + | | group1 = [[Thrombocytosis]] | ||
| + | | list1 = [[Essential thrombocytosis]] | ||
| + | |||
| + | | group2 = [[Hypercoagulability]] | ||
| + | | list2 = ''primary:'' [[Antithrombin III deficiency]]{{·}} [[Protein C deficiency]]/[[Activated protein C resistance]]/[[Protein S deficiency]]/[[Factor V Leiden]]{{·}} [[Hyperprothrombinemia]] <BR>''acquired:'' [[Disseminated intravascular coagulation|DIC]] ([[Congenital afibrinogenemia]], [[Purpura fulminans]]){{·}} ''[[autoimmune]]'' ([[Antiphospholipid syndrome|Antiphospholipid]]) | ||
| + | |||
| + | }} | ||
| + | |||
| + | | group2 = ↓ | ||
| + | | list2 = {{Navbox subgroup | ||
| + | | groupstyle = background-color: MistyRose; | ||
| + | |||
| + | |group1 = [[Thrombocytopenia]]<br/>and [[purpura]] | ||
| + | |list1 = [[Nonthrombocytopenic purpura]]: [[Henoch-Schönlein purpura]] | ||
| + | |||
| + | [[Thrombocytopenic purpura]]: [[Idiopathic thrombocytopenic purpura|ITP]] ([[Evans syndrome]]){{·}} [[Thrombotic microangiopathy|TM]] ([[Thrombotic thrombocytopenic purpura|TTP]]) | ||
| + | |||
| + | [[Heparin-induced thrombocytopenia]]{{·}} [[May-Hegglin anomaly]] | ||
| + | |||
| + | | group2 = [[Platelet#Diseases|Platelet function]] | ||
| + | | list2 = ''adhesion'' ([[Bernard-Soulier syndrome]]){{·}} ''aggregation'' ([[Glanzmann's thrombasthenia]]){{·}} ''[[platelet storage pool deficiency]]'' ([[Hermansky-Pudlak syndrome]], [[Gray platelet syndrome]]) | ||
| + | |||
| + | | group3 = [[Clotting factor]] | ||
| + | | list3 = [[Haemophilia|Hemophilia]] ([[Haemophilia A|A/VIII]], [[Haemophilia B|B/IX]], [[Haemophilia C|C/XI]]) • [[Von Willebrand disease]] • [[Hypoprothrombinemia|Hypoprothrombinemia/II]]{{·}} [[Factor XIII deficiency|XIII]] | ||
| + | |||
| + | }} | ||
| + | |||
| + | }} | ||
| + | |||
| + | |||
| + | |||
| + | | below = {{Myeloid navs}} | ||
| + | |||
| + | }} | ||
| + | <includeonly>[[Category:Hematology]]</includeonly> | ||
| + | <noinclude> | ||
| + | ''This template is part of the [[Wikipedia:Navigational templates#Medicine|Medical series]] of [[Wikipedia:Navigational templates|navigation boxes]]. Refer to [[Template:Medicine]] and its [[Template_talk:Medicine|talk page]] for suggestions on style and editing.'' | ||
| + | |||
| + | [[Category:Myeloid disease and disorder templates]] | ||
| + | |||
| + | [[ar:قالب:Hematology]] | ||
| + | [[bn:টেমপ্লেট:রক্তবিদ্যা]] | ||
| + | [[fr:Modèle:Hématologie]] | ||
| + | </noinclude> | ||
Revision as of 16:15, 9 February 2011
This template is part of the Medical series of navigation boxes. Refer to Template:Medicine and its talk page for suggestions on style and editing.
ar:قالب:Hematology bn:টেমপ্লেট:রক্তবিদ্যা fr:Modèle:Hématologie