# LADD syndrome

> autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes

**Wikidata**: [Q18553246](https://www.wikidata.org/wiki/Q18553246)  
**Source**: https://4ort.xyz/entity/ladd-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. LADD syndrome is caused by FGF10 mutations
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000070193/MONDO_0007872)
6. Mutations in different components of FGF signaling in LADD syndrome
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000066468/MONDO_0007872)
8. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000066468/Orphanet_2363)
9. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000068078/MONDO_0007872)
10. [Identifiers.org](https://registry.identifiers.org/registry/doid)