LVNC2
MCID: LFT011
MIFTS: 18

Left Ventricular Noncompaction 2 (LVNC2)

Categories: Blood diseases, Cardiovascular diseases, Fetal diseases, Genetic diseases, Rare diseases

Aliases & Classifications for Left Ventricular Noncompaction 2

MalaCards integrated aliases for Left Ventricular Noncompaction 2:

Name: Left Ventricular Noncompaction 2 56 13 6 71
Lvnc2 56

Classifications:



External Ids:

OMIM 56 609470
OMIM Phenotypic Series 56 PS604169
UMLS 71 C1836118

Summaries for Left Ventricular Noncompaction 2

MalaCards based summary : Left Ventricular Noncompaction 2, also known as lvnc2, is related to left ventricular noncompaction and third-degree atrioventricular block. An important gene associated with Left Ventricular Noncompaction 2 is LVNC2 (Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 2). Affiliated tissues include heart and testes.

More information from OMIM: 609470 PS604169

Related Diseases for Left Ventricular Noncompaction 2

Graphical network of the top 20 diseases related to Left Ventricular Noncompaction 2:



Diseases related to Left Ventricular Noncompaction 2

Symptoms & Phenotypes for Left Ventricular Noncompaction 2

Clinical features from OMIM:

609470

Drugs & Therapeutics for Left Ventricular Noncompaction 2

Search Clinical Trials , NIH Clinical Center for Left Ventricular Noncompaction 2

Genetic Tests for Left Ventricular Noncompaction 2

Anatomical Context for Left Ventricular Noncompaction 2

MalaCards organs/tissues related to Left Ventricular Noncompaction 2:

40
Heart, Testes

Publications for Left Ventricular Noncompaction 2

Articles related to Left Ventricular Noncompaction 2:

(showing 3, show less)
# Title Authors PMID Year
1
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). 6
21810866 2011
2
Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15. 56
15173023 2004
3
Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients. 56
12749056 2003

Variations for Left Ventricular Noncompaction 2

ClinVar genetic disease variations for Left Ventricular Noncompaction 2:

6 (showing 1, show less) ‎‎
# Gene Name Type Significance ClinVarId dbSNP ID GRCh37 Pos GRCh38 Pos
1 TTN NM_001267550.2(TTN):c.75727G>T (p.Glu25243Ter)SNV Likely pathogenic 265826 rs1114167338 2:179435132-179435132 2:178570405-178570405

Expression for Left Ventricular Noncompaction 2

Search GEO for disease gene expression data for Left Ventricular Noncompaction 2.

Pathways for Left Ventricular Noncompaction 2

GO Terms for Left Ventricular Noncompaction 2

Sources for Left Ventricular Noncompaction 2

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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