# von Willebrand's disease 2

> von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has material basis in mutation in the VWF gene which maps to chromosome 12p13

**Wikidata**: [Q26492789](https://www.wikidata.org/wiki/Q26492789)  
**Source**: https://4ort.xyz/entity/von-willebrand-s-disease-2


## References

1. Disease Ontology
2. Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type IIA von Willebrand factor
3. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000110799/Orphanet_166081)
4. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)