RCM2
MCID: CRD057
MIFTS: 19

Cardiomyopathy, Familial Restrictive, 2 (RCM2)

Categories: Cardiovascular diseases, Genetic diseases, Rare diseases

Aliases & Classifications for Cardiomyopathy, Familial Restrictive, 2

MalaCards integrated aliases for Cardiomyopathy, Familial Restrictive, 2:

Name: Cardiomyopathy, Familial Restrictive, 2 57 13 70
Restrictive Cardiomyopathy 2 12 15
Rcm2 57 12
Cardiomyopathy, Restrictive, Familial, Type 2 39
Familial Restrictive Cardiomyopathy 2 12

Classifications:



External Ids:

Disease Ontology 12 DOID:0111426
OMIM® 57 609578
OMIM Phenotypic Series 57 PS115210
MedGen 41 C1865071
UMLS 70 C1865071

Summaries for Cardiomyopathy, Familial Restrictive, 2

Disease Ontology : 12 A restrictive cardiomyopathy that has material basis in variation in a region on chromosome 10q23.3.

MalaCards based summary : Cardiomyopathy, Familial Restrictive, 2, also known as restrictive cardiomyopathy 2, is related to restrictive cardiomyopathy and myopathy, spheroid body. An important gene associated with Cardiomyopathy, Familial Restrictive, 2 is RCM2 (Cardiomyopathy, Familial Restrictive, 2).

More information from OMIM: 609578 PS115210

Related Diseases for Cardiomyopathy, Familial Restrictive, 2

Graphical network of the top 20 diseases related to Cardiomyopathy, Familial Restrictive, 2:



Diseases related to Cardiomyopathy, Familial Restrictive, 2

Symptoms & Phenotypes for Cardiomyopathy, Familial Restrictive, 2

Clinical features from OMIM®:

609578 (Updated 20-May-2021)

Drugs & Therapeutics for Cardiomyopathy, Familial Restrictive, 2

Search Clinical Trials , NIH Clinical Center for Cardiomyopathy, Familial Restrictive, 2

Genetic Tests for Cardiomyopathy, Familial Restrictive, 2

Anatomical Context for Cardiomyopathy, Familial Restrictive, 2

Publications for Cardiomyopathy, Familial Restrictive, 2

Articles related to Cardiomyopathy, Familial Restrictive, 2:

# Title Authors PMID Year
1
Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locus. 57
16061566 2005
2
Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathy. 57
11298680 2001
3
Palmitoylation of CM2 is dispensable to influenza C virus replication. 61
21352864 2011
4
[Radiation exposure and radiation risk in angiocardiography in adults]. 61
6500485 1984
5
[Radiation dose in abdominal examinations with whole body computer tomography (author's transl)]. 61
424670 1979
6
[Radiation dose and risk in gastrointestinal roentgendiagnostic of the child (author's transl)]. 61
568682 1978

Variations for Cardiomyopathy, Familial Restrictive, 2

Expression for Cardiomyopathy, Familial Restrictive, 2

Search GEO for disease gene expression data for Cardiomyopathy, Familial Restrictive, 2.

Pathways for Cardiomyopathy, Familial Restrictive, 2

GO Terms for Cardiomyopathy, Familial Restrictive, 2

Molecular functions related to Cardiomyopathy, Familial Restrictive, 2 according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 cytoskeletal protein binding GO:0008092 8.62 MYPN FLNC

Sources for Cardiomyopathy, Familial Restrictive, 2

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
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
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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