A rare, genetic, isolated constitutional thrombocytopenia disease characterized by impaired platelet aggregation resulting from a defect in thromboxane synthesis or signaling, manifesting with mild to moderate mucocutaneous, gastrointestinal or surgical bleeding (e.g. easy bruising, prolonged epistaxis, excessive bleeding after a tooth extraction).
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gray platelet syndrome
MONDO:0007686
primary release disorder of platelets
MONDO:0008309
platelet-type von Willebrand disease
MONDO:0008332
platelet-type bleeding disorder 16
MONDO:0008552
platelet-type bleeding disorder 17
MONDO:0008553
Ehlers-Danlos syndrome, fibronectinemic type
MONDO:0009158