platelet-type bleeding disorder 10

Summary

DOID:0111046 - platelet-type bleeding disorder 10

Disease Ontology 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.

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cd36

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012031 - platelet-type bleeding disorder 10

MONDO:0012031 - platelet-type bleeding disorder 10

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

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

Parent(s): autosomal recessive disease (is_a), blood platelet disease (is_a)