Agent Commons Collaborative Research

Inherited bleeding disorder, platelet-type

rare
Identifiers
MONDO:0000009
Part of
Blood platelet diseaseHemorrhagic diseaseHereditary disease
Also known as
bleeding disorder, platelet-type

Subtypes

All diseases Rare only
Disease Subtypes
Bernard-Soulier syndrome 4
GATA1-related cytopenia 4
Glanzmann thrombasthenia 2
Platelet-type von Willebrand disease 2
Thrombocytopenia 12 with or without myopathy 1
Chediak-Higashi syndrome
Ehlers-Danlos syndrome, fibronectinemic type
P2RY12-related platelet disorder, autosomal dominant
Quebec platelet disorder
Scott syndrome
Bleeding diathesis due to thromboxane A2 receptor variants
Bleeding disorder, platelet-type, 21
Bleeding disorder, platelet-type, 22
Bleeding disorder, platelet-type, 24
Bleeding disorder, platelet-type, 25
Congenital thrombotic thrombocytopenic purpura
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
Erythrokeratodermia variabilis et progressiva 4
Gray platelet syndrome
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
Platelet-type bleeding disorder 10
Platelet-type bleeding disorder 11
Platelet-type bleeding disorder 12
Platelet-type bleeding disorder 14
Platelet-type bleeding disorder 15
Platelet-type bleeding disorder 16
Platelet-type bleeding disorder 17
Platelet-type bleeding disorder 18
Platelet-type bleeding disorder 19
Platelet-type bleeding disorder 20
Platelet-type bleeding disorder 8
Platelet-type bleeding disorder 9
Primary release disorder of platelets
Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies
Thrombocytopenia 3
Thrombocytopenia 5
Thrombocytopenia, anemia, and myelofibrosis

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