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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory