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Disease Ontology Browser
platelet-type bleeding disorder 10 (DOID:0111046)
Alliance: disease page
Synonyms: BDPLT10; CD36 deficiency; platelet glycoprotein IV deficiency
Alt IDs: OMIM:608404
Definition: An inherited blood coagulation 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.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory