FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term platelet-type bleeding disorder 10 ID (Ontology) DOID:0111046 (Human Disease)
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.
Also Known As "BDPLT10" ; "CD36 deficiency" ; "platelet glycoprotein IV deficiency"
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 Genes
 platelet-type bleeding disorder 10       2
 for disease ribbon | platelet-type bleeding disorder 10       2
 model of | platelet-type bleeding disorder 10       2
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autosomal genetic disease
 |__autosomal recessive disease__
blood coagulation disease        |
 |__blood platelet disease_______|
                                 platelet-type bleeding disorder 10  2 rec.
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Is a autosomal recessive disease
blood platelet disease
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Synonyms
  • "BDPLT10" EXACT OMO:0003012
    "CD36 deficiency" EXACT
    "platelet glycoprotein IV deficiency" EXACT
Secondary IDs
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MIM:608404