Disease Browser
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Parent Node: Blood Platelet Disorders (D001791) |
..Starting node ..Platelet Prostacyclin Receptor Defect (C564884)
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Child Nodes:
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Sister Nodes: |
..Bernard-Soulier Syndrome (D001606) 5
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..BLEEDING DISORDER, PLATELET-TYPE, 8 (OMIM:609821)
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..Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality (C565600)
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..Gray Platelet Syndrome (D055652) 1
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..Platelet Aggregation, Spontaneous (C566800)
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..Platelet Disorder, Familial, with Associated Myeloid Malignancy (C563324)
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..Platelet Disorder, Undefined (C566799)
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..Platelet Factor 3 Deficiency (C566798)
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..Platelet Glycoprotein IV Deficiency (C564245)
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..Platelet Prostacyclin Receptor Defect (C564884)
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..Platelet Receptor for Collagen, Deficiency of (C565999)
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..Platelet Signal Processing Defect (C566796)
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..Platelet Storage Pool Deficiency (D010981) 5
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..Primary Release Disorder Of Platelets (C566759)
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..Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet (C567786)
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..Stormorken Syndrome (C566108)
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..Thrombasthenia (D013915) 3
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..Thrombocytopenia (D013921) 48
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..Thrombocytosis (D013922) 4
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..Thromboxane Synthetase Deficiency (C562866)
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..von Willebrand Diseases (D014842) 6
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..White platelet syndrome (C536702)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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