# 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

**Wikidata**: [Q32146609](https://www.wikidata.org/wiki/Q32146609)  
**Source**: https://4ort.xyz/entity/platelet-type-bleeding-disorder-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/8fef91aa-8c41-4044-b601-da24c2bab351--2020-05-27T16:00:00)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_8fef91aa-8c41-4044-b601-da24c2bab351-2020-05-27T160000.000Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000185245/MONDO_0008332)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)