platelet-type bleeding disorder 3
inherited blood coagulation disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has material basis in mutation in the GP1BA gene on chromosome 17p13.2
Press Enter · cited answer in seconds
0 sources
platelet-type bleeding disorder 3
Summary
platelet-type bleeding disorder 3 is a rare disease[1]. It is known by 12 alternative names across languages and contexts.[2]
Key Facts
- platelet-type bleeding disorder 3's instance of is recorded as rare disease[3].
- platelet-type bleeding disorder 3's instance of is recorded as class of disease[4].
- platelet-type bleeding disorder 3 is a type of inherited blood coagulation disease[5].
- platelet-type bleeding disorder 3 is a type of rare hemorrhagic disorder due to a qualitative platelet defect[6].
- platelet-type bleeding disorder 3 is a type of autosomal dominant disease[7].
- platelet-type bleeding disorder 3 is a type of blood platelet disease[8].
- platelet-type bleeding disorder 3's NCI Thesaurus ID is recorded as C131681[9].
- platelet-type bleeding disorder 3's genetic association is recorded as GP1BA[10].
- platelet-type bleeding disorder 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111056[11].
- platelet-type bleeding disorder 3's exact match is recorded as http://identifiers.org/doid/DOID:0111056[12].
- platelet-type bleeding disorder 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_52530[13].
- platelet-type bleeding disorder 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
platelet-type bleeding disorder 3 is known by 12 alternative names across languages and contexts.[2]