Human genes for platelet-type bleeding disorder 10
Platelet-type bleeding disorder 10 [DOID:0111046]
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.
Synonyms: platelet-type bleeding disorder 10, DOID:0111046, platelettype bleeding disorder 10, BDPLT10, CD36 deficiency ...