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Disease Ontology Browser
Bernard-Soulier syndrome (DOID:2217)
Alliance: disease page
Synonyms: Bernard - Soulier thrombopathy; Bernard Soulier syndrome; Giant platelet syndrome; Hemorrhagic dystrophic thrombocytopenia; Thrombopathy, Bernard-Soulier
Alt IDs: OMIM:231200, MESH:D001606, NCI:C84595, ORDO:274, UMLS_CUI:C0005129
Definition: An inherited blood coagulation disease characterized by autosomal recessive inheritance of mucosal bleeding, purpuric skin bleeding, epistaxis, and menorrhagia with prolonged bleeding times, enlarged platelets and absence of platelet aggregation in response to von Willebrand factor that has material_basis_in mutation in the GP1BA gene, the GP1BB gene, or the GP9 gene which are subunits of the platelet membrane von Willebrand factor receptor complex, glycoprotein Ib.

Disease References using Mouse Models (3)

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
02/18/2020
MGI 6.14
The Jackson Laboratory