# Jervell-Lange Nielsen syndrome

> Human disease

**Wikidata**: [Q3304152](https://www.wikidata.org/wiki/Q3304152)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Jervell_and_Lange-Nielsen_syndrome)  
**Source**: https://4ort.xyz/entity/jervell-lange-nielsen-syndrome


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. Freebase Data Dumps. 2013
4. Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000180509/MONDO_0002441)
6. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
7. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_2cb5cd32-6663-48bc-b8b0-3b9ca34e2cb7-2017-12-19T050000.000Z)
8. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000053918/MONDO_0002441)
9. [Identifiers.org](https://registry.identifiers.org/registry/doid)