# von Willebrand's disease 1

> von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has material basis in heterozygous mutation in the VWF gene on chromosome 12p13

**Wikidata**: [Q26492788](https://www.wikidata.org/wiki/Q26492788)  
**Source**: https://4ort.xyz/entity/von-willebrand-s-disease-1


## References

1. Disease Ontology
2. A database of polymorphisms in the von Willebrand factor gene and pseudogene. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of th
3. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000110799/Orphanet_166078)
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)