| Metadata | |
|---|---|
| ID | DOID:0111056 |
| Name | platelet-type bleeding disorder 3 |
| Definition | A blood platelet 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. https://www.ncbi.nlm.nih.gov/pubmed/8486780, https://www.ncbi.nlm.nih.gov/pubmed/2052556 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
BDPLT3 [EXACT] platelet type-von Willebrand disease [EXACT] pseudo-von Willebrand disease [EXACT] PT-VWD [EXACT] von Willebrand disease platelet-type [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |