CMD1Q
MCID: CRD071
MIFTS: 15

Cardiomyopathy, Dilated, 1q (CMD1Q)

Categories: Blood diseases, Cardiovascular diseases, Ear diseases, Genetic diseases, Immune diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Cardiomyopathy, Dilated, 1q

MalaCards integrated aliases for Cardiomyopathy, Dilated, 1q:

Name: Cardiomyopathy, Dilated, 1q 58 13 74
Cmd1q 58 12
Dilated Cardiomyopathy 1q 12

Classifications:



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Disease Ontology 12 DOID:0110442
OMIM 58 609915
ICD10 34 I42.0
MedGen 43 C1835926
UMLS 74 C1835926

Summaries for Cardiomyopathy, Dilated, 1q

Disease Ontology : 12 A dilated cardiomyopathy that has material basis in variation in the chromosome region 7q22.3-q31.1.

MalaCards based summary : Cardiomyopathy, Dilated, 1q, also known as cmd1q, is related to cone-rod dystrophy and hearing loss 2. An important gene associated with Cardiomyopathy, Dilated, 1q is CMD1Q (Cardiomyopathy, Dilated 1Q (Autosomal Dominant)).

Description from OMIM: 609915

Related Diseases for Cardiomyopathy, Dilated, 1q

Symptoms & Phenotypes for Cardiomyopathy, Dilated, 1q

Clinical features from OMIM:

609915

Drugs & Therapeutics for Cardiomyopathy, Dilated, 1q

Search Clinical Trials , NIH Clinical Center for Cardiomyopathy, Dilated, 1q

Genetic Tests for Cardiomyopathy, Dilated, 1q

Anatomical Context for Cardiomyopathy, Dilated, 1q

Publications for Cardiomyopathy, Dilated, 1q

Variations for Cardiomyopathy, Dilated, 1q

Expression for Cardiomyopathy, Dilated, 1q

Search GEO for disease gene expression data for Cardiomyopathy, Dilated, 1q.

Pathways for Cardiomyopathy, Dilated, 1q

GO Terms for Cardiomyopathy, Dilated, 1q

Sources for Cardiomyopathy, Dilated, 1q

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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