# Coffin-Lowry syndrome

> genetic disorder that is X-linked dominant

**Wikidata**: [Q1106881](https://www.wikidata.org/wiki/Q1106881)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Coffin–Lowry_syndrome)  
**Source**: https://4ort.xyz/entity/coffin-lowry-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. [Source](https://ddrare.nibiohn.go.jp/)
3. Disease Ontology
4. Freebase Data Dumps. 2013
5. UniProt
6. Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome
7. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/af32a931-1d55-432f-82cf-ce87f6c26580--2019-05-28T04:00:00)
8. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_af32a931-1d55-432f-82cf-ce87f6c26580-2019-05-28T040000.000Z)
9. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000177189/MONDO_0010561)
10. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)