Left ventricular noncompaction 2

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr:
OMIM Id: 609470
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant
Age of onset: All ages

Disease classification (adopted from Orphanet):

Parent Diseases: Left ventricular noncompaction
 -Rare cardiac disease
 -Rare genetic disease

Comment:

Left ventricular noncompaction 2 is associated with LVNC-105 locus (chromosome 11p15) (PMID:15173023).

Symptom Information: Sort by abundance 

1
 (HPO:0001642) Pulmonic stenosis 15173023 IBIS 89 / 7739
2
 (HPO:0001635) Congestive heart failure 15173023 IBIS 232 / 7739
3
 (HPO:0001634) Mitral valve prolapse 15173023 IBIS 69 / 7739
4
 (HPO:0001645) Sudden cardiac death 15173023 IBIS 84 / 7739
5
 (HPO:0011664) Left ventricular noncompaction cardiomyopathy 15173023 IBIS 10 / 7739
6
 (MedDRA:10007625) Cardiogenic shock 15173023 IBIS 1 / 7739
7
 (OMIM) Prominent endomyocardial trabeculations 15173023 IBIS 3 / 7739

Associated genes:

LVNC-105 locus (11p15)

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: