CHDS7
MCID: CRN177
MIFTS: 10

Coronary Heart Disease 7 (CHDS7)

Categories: Genetic diseases

Aliases & Classifications for Coronary Heart Disease 7

MalaCards integrated aliases for Coronary Heart Disease 7:

Name: Coronary Heart Disease 7 57 75 29 6
Coronary Heart Disease, Susceptibility to, 7 57 13
Chds7 57 75
Heart, Coronary, Disease, Susceptibility to, Type 7 40

Classifications:



External Ids:

OMIM 57 610938
MedGen 42 C1970441
MeSH 44 D003327

Summaries for Coronary Heart Disease 7

UniProtKB/Swiss-Prot : 75 Coronary heart disease 7: A multifactorial disease characterized by an imbalance between myocardial functional requirements and the capacity of the coronary vessels to supply sufficient blood flow. Decreased capacity of the coronary vessels is often associated with thickening and loss of elasticity of the coronary arteries.

MalaCards based summary : Coronary Heart Disease 7, is also known as coronary heart disease, susceptibility to, 7. An important gene associated with Coronary Heart Disease 7 is CD36 (CD36 Molecule). Affiliated tissues include heart.

Description from OMIM: 610938

Related Diseases for Coronary Heart Disease 7

Symptoms & Phenotypes for Coronary Heart Disease 7

Clinical features from OMIM:

610938

Drugs & Therapeutics for Coronary Heart Disease 7

Search Clinical Trials , NIH Clinical Center for Coronary Heart Disease 7

Genetic Tests for Coronary Heart Disease 7

Genetic tests related to Coronary Heart Disease 7:

# Genetic test Affiliating Genes
1 Coronary Heart Disease 7 29 CD36

Anatomical Context for Coronary Heart Disease 7

MalaCards organs/tissues related to Coronary Heart Disease 7:

41
Heart

Publications for Coronary Heart Disease 7

Variations for Coronary Heart Disease 7

ClinVar genetic disease variations for Coronary Heart Disease 7:

6 (show all 12)
# Gene Variation Type Significance SNP ID Assembly Location
1 CD36 NM_001001547.2(CD36): c.429+2T> C single nucleotide variant Likely pathogenic rs3211893 GRCh37 Chromosome 7, 80290528: 80290528
2 CD36 NM_001001547.2(CD36): c.429+2T> C single nucleotide variant Likely pathogenic rs3211893 GRCh38 Chromosome 7, 80661212: 80661212
3 CD36 NM_001001547.2(CD36): c.701_701+3dup duplication Likely benign GRCh38 Chromosome 7, 80664497: 80664500
4 CD36 NM_001001547.2(CD36): c.701_701+3dup duplication Likely benign GRCh37 Chromosome 7, 80293813: 80293816
5 CD36 NM_001001547.2(CD36): c.1254+1G> A single nucleotide variant Likely pathogenic rs148051111 GRCh37 Chromosome 7, 80302726: 80302726
6 CD36 NM_001001547.2(CD36): c.1254+1G> A single nucleotide variant Likely pathogenic rs148051111 GRCh38 Chromosome 7, 80673410: 80673410
7 CD36 NM_001001547.2(CD36): c.-184+11225A> G single nucleotide variant no interpretation for the single variant rs1984112 GRCh38 Chromosome 7, 80613604: 80613604
8 CD36 NM_001001547.2(CD36): c.-184+11225A> G single nucleotide variant no interpretation for the single variant rs1984112 GRCh37 Chromosome 7, 80242920: 80242920
9 CD36 -31118A-G single nucleotide variant no interpretation for the single variant rs1761667
10 CD36 25444G-A single nucleotide variant no interpretation for the single variant
11 CD36 30294C-G single nucleotide variant no interpretation for the single variant rs1049673
12 CD36 27645del/ins indel no interpretation for the single variant

Expression for Coronary Heart Disease 7

Search GEO for disease gene expression data for Coronary Heart Disease 7.

Pathways for Coronary Heart Disease 7

GO Terms for Coronary Heart Disease 7

Sources for Coronary Heart Disease 7

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
Content
Loading form....