Summary Literature (0)

DOID:0111046 - platelet-type bleeding disorder 10

Disease Ontology 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.

Synonyms: BDPLT10, CD36 deficiency, platelet glycoprotein IV deficiency,

Echinobase Genes :


OMIM:

MIM:608404 - platelet glycoprotein iv deficiency

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee