# anterior segment dysgenesis 7

> human disease

**Wikidata**: [Q55998736](https://www.wikidata.org/wiki/Q55998736)  
**Source**: https://4ort.xyz/entity/anterior-segment-dysgenesis-7


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000130508/MONDO_0010015)
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000130508/Orphanet_289499)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)