Jervell-Lange Nielsen syndrome
Information
- Disease name
- Jervell-Lange Nielsen syndrome
- Disease ID
- DOID:2842
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT05687474 | Recruiting | Baby Detect : Genomic Newborn Screening | September 1, 2022 | August 31, 2025 |
- Disase is a (Disease Ontology)
- DOID:2843
- Cross Reference ID (Disease Ontology)
- GARD:3048
- Cross Reference ID (Disease Ontology)
- MESH:D029593
- Cross Reference ID (Disease Ontology)
- MIM:220400
- Cross Reference ID (Disease Ontology)
- MIM:612347
- Cross Reference ID (Disease Ontology)
- NCI:C84793
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:49518001
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0022387
- Exact Synonym (Disease Ontology)
- Jervell and Lange-Nielson syndrome
- MeSH unique ID (MeSH (Medical Subject Headings))
- D029593