Grey platelet syndrome
Classification & external resources
|ICD-10 ||D69.1 |
|OMIM ||139090 |
|DiseasesDB ||29160 |
Grey platelet syndrome is a rare condition caused by a reduction or absence of the platelet alpha-granules in blood platelet, or of the proteins contained in these granules. The International Statistical Classification of Diseases and Related Health Problems (most commonly known by the abbreviation ICD) provides codes to classify diseases and a wide variety of signs, symptoms, abnormal findings, complaints, social circumstances and external causes of injury or disease. ...
The International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings, complaints, social circumstances and external causes of injury or diseases, as classified by the World Health Organization (WHO). ...
// C00-D48 - Neoplasms (C00-C14) Malignant neoplasms, lip, oral cavity and pharynx (C00) Malignant neoplasm of lip (C01) Malignant neoplasm of base of tongue (C02) Malignant neoplasm of other and unspecified parts of tongue (C03) Malignant neoplasm of gum (C04) Malignant neoplasm of floor of mouth (C05) Malignant neoplasm of...
The Mendelian Inheritance in Man project is a database that catalogues all the known diseases with a genetic component, and - when possible - links them to the relevant genes in the human genome. ...
The Disease Bold textDatabase is a free website that provides information about the relationships between medical conditions, symptoms, and medications. ...
A 250 ml bag of newly collected platelets. ...
- Pseudo gray platelet syndrome
- "The gray platelet syndrome: clinical spectrum of the disease.". Blood Rev. PMID 16442192.
Pathology: hematology/hematological malignancy (primarily C81-C96/200-208, D45-D47, D50-D77/280-289)
|WBCs ||Lymphoid: Lymphoid leukemia (ALL, CLL, HCL) • Lymphoma (Hodgkin's disease, NHL) • LPD • Myeloma (Multiple myeloma, Extramedullary plasmacytoma) |
Myeloid: Myeloid leukemia (AML, CML) • MPD Ph- (Essential thrombocytosis, Polycythemia vera, Myelofibrosis) • MDS
-cytosis (Agranulocytosis, Leukocytosis, Lymphocytosis, Monocytosis, Eosinophilia) • -penia (Lymphopenia, Neutropenia)
|RBCs/anemia/hemoglobinopathy ||Nutritional anemia: Iron deficiency anemia, Plummer-Vinson syndrome, Pernicious anemia, Megaloblastic anemia |
Hereditary hemolytic anemia: G6PD Deficiency, Thalassemia, Sickle-cell disease/trait, Hereditary spherocytosis, Hereditary elliptocytosis, Hereditary stomatocytosis
Acquired hemolytic anemia: Warm autoimmune hemolytic anemia, HUS, MAHA, PNH
Aplastic anemia: Acquired PRCA, Fanconi anemia • Hemochromatosis
|Coagulation/platelets ||Coagulopathy: DIC • Hemophilia (A, B, C) • Von Willebrand disease |
Purpura: Henoch-Schönlein, ITP, TTP
Other hemorrhagic conditions: Bernard-Soulier syndrome - Glanzmann's thrombasthenia - Grey platelet syndrome
|other ||Methemoglobinemia - Langerhans cell histiocytosis |