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Glanzmann Thrombasthenia
Glanzmann thrombasthenia
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Blood disorders
(8)
Bernard-soulier syndrome
Essential thrombocytopenia
Hematology
Leukemia
Myelofibrosis
Myelofibrosis
Von willebrand disease
Hemophilia
Hemophilia a
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Genetic disorders
(15)
Sly syndrome
Thymic aplasia
Refractory anemia with ringed sideroblasts
Trichorhin- ophalangeal syndrome
Hurler-Scheie Syndrome
Hurler-Scheie Syndrome
Trisomy 22
Trisomy 9
Nevoid basal cell carcinoma syndrome
Tetrasomy
Partial trisomy
Severe combined immunodeficiency
Bernard-soulier syndrome
Von willebrand disease
Hemophilia
Hemophilia a
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Autosomal recessive disorders
Sly syndrome
Bernard-soulier syndrome
Hurler-Scheie Syndrome
Rare diseases
Naegeli syndrome
Sly syndrome
Severe combined immunodeficiency
Medical condition
(34)
Thrombasthenia of glanzmann and naegeli
Lymphohistiocytosis
Reticular dysgenesis
Acute biphenotypic leukemia
Platelet
Platelet
Neuraminidase deficiency
Giant cell glioblastoma
Glycogenosis
Thrombosis
Talipes
Gastric cancer
Factor viia
Malignancies
Epistaxis
Factor xa
Thyroid cancer
Torn meniscus
Naegeli syndrome
Sly syndrome
Thymic aplasia
Refractory anemia with ringed sideroblasts
Trichorhin- ophalangeal syndrome
Bernard-soulier syndrome
Essential thrombocytopenia
Hurler-Scheie Syndrome
Leukemia
Trisomy 9
Nevoid basal cell carcinoma syndrome
Myelofibrosis
Partial trisomy
Von willebrand disease
Hemophilia
Severe combined immunodeficiency
Hemophilia a
more...
Syndromes
Naegeli syndrome
Sly syndrome
Thymic aplasia
Hurler-Scheie Syndrome
Coagulation system
(33)
Clot retraction
Factor viii
Fibrinogen
Haemostasis
Thrombin
Thrombin
Tissue factor
Von willebrand factor
Antithrombin
Bone hemostasis
Coagulation
Cofact
Des-gamma carboxyprothrombin
Factor IX
Factor XI
Factor XII
Factor XIII
Factor viia
Factor xa
Fibrinogenolysis
High-molec- ular-weight kininogen
Human Activated Protein C
Medical Laboratory Scientist
Platelet
Platelet activation
Prekallikrein
Protein C
Protein S
Protein Z
Protein Z-related protease inhibitor
Prothrombin complex concentrate
Prothrombinase
Thrombomodulin
Tissue factor pathway inhibitor
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Lysosomal storage diseases
(40)
Mucolipidosis II
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler-Scheie Syndrome
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuraminidase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sly syndrome
Tay-Sachs disease
Wolman disease
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See also
(20)
Diseases and disorders
Refractory anemia with excess blasts in transformation
Platelet membrane glycoprotein
Glycoprotein IIb/IIIa
GPIIb
GPIIb
Integrin
Telecanthus
Glycoprotein
Juvenile Myelomonocytic Leukemia (JMML)
Ristocetin
Glycoprotein Ib
Blood diseases
Coagulation disorder
Autosomal recessive
Hemorrhagic
Glycoprotein IIb/IIIa inhibitors
Prolonged bleeding
Platelet aggregation
Vibration white finger
Cord blood bank
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