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DOID:0111908 - thrombophilia due to thrombomodulin defect
Disease Ontology Definition:A thrombophilia characterized by increased risk of developing arterial but not venous thrombosis that has_material_basis_in mutation in the THBD gene on chromosome 20p11.21.
Synonyms: THBD-related bleeding disorder, THBD-related coagulopathy, THPH12, thrombomodulin-related bleeding disorder, thrombomodulin-related coagulopathy,
Xenbase Genes
:
thbd
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal genetic disease (is_a),
thrombophilia (is_a)