Search Ontology:
Human Disease

platelet-type bleeding disorder 10

Term ID
DOID:0111046
Synonyms
  • BDPLT10
  • CD36 deficiency
  • platelet glycoprotein IV deficiency
Definition
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. (3)
References
Ontology
Human Disease   ( DOID:0111046 )
Relationships
is a type of
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Genes Involved
Zebrafish Models