platelet-type bleeding disorder 10
A blood platelet disease characterized by autosomal recessive inheritance of variable bleeding tendency, thrombocytopenia, giant platelets, and prolonged bleeding times that has_material_basis_in homozygous or compound heterozygous mutation in the CD36 antigen gene on chromosome 7q21.
Exact Synonyms
BDPLT10
CD36 deficiency
platelet glycoprotein IV deficiency
class Information
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has_obo_namespace
disease_ontology
class Relations
Disjoint with
- platelet-type bleeding disorder 16
- platelet-type bleeding disorder 8
- gray platelet syndrome
- platelet-type bleeding disorder 9
- platelet-type bleeding disorder 14
- platelet-type bleeding disorder 19
- platelet-type bleeding disorder 17
- Quebec platelet disorder
- platelet-type bleeding disorder 18
- Scott syndrome
- hemophilia B
- von Willebrand's disease
- factor XIII deficiency
- factor VII deficiency
- factor V deficiency
- Bernard-Soulier syndrome
- Glanzmann's thrombasthenia
- factor X deficiency
- congenital afibrinogenemia
- antithrombin III deficiency
- protein C deficiency