# autosomal dominant retinal vasculopathy with cerebral leukodystrophy

> human disease

**Wikidata**: [Q18209717](https://www.wikidata.org/wiki/Q18209717)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-retinal-vasculopathy-with-cerebral-leukodystrophy


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000213689/MONDO_0008641)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000213689/Orphanet_3421)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000213689/Orphanet_71291)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)