hereditary bleeding disorder
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Introduction
Also see platelet disorder, coagulation disorder
Genetics
- associated with defects in P2RX1[1]
- associated with defects in P2RY12[2]
- associated with defects in TBXA2R[3], autosomal dominant
More general terms
- risk for hemorrhage; hemorrhagic diathesis; bleeding disorder
- genetic disease of the blood/bone marrow
References
- ↑ 1.0 1.1 OMIM https://mirror.omim.org/entry/600845
- ↑ 2.0 2.1 OMIM https://mirror.omim.org/entry/609821
- ↑ 3.0 3.1 OMIM https://mirror.omim.org/entry/188070
- ↑ Boender J, Kruip MJ, Leebeek FW. A diagnostic approach to mild bleeding disorders. J Thromb Haemost. 2016;14:1507-1516. PMID: https://pubmed.ncbi.nlm.nih.gov/27208505