von Willebrand's disease 1 Disease Ontology Browser

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Disease Ontology Browser

von Willebrand's disease 1 (DOID:0060573)
Alliance: disease page
Synonyms: von Willebrand disease type 1; von Willebrand disease type I; VWD1; VWD type 1
Alt IDs: OMIM:193400, ICD10CM:D68.01, MESH:D056725, NCI:C131685, UMLS_CUI:C1264039
Definition: A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has_material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13.

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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