Preferred Label : Coronary heart disease, susceptibility to, 1;
CISMeF acronym : CHDS1;
Type : Phenotype or locus, molecular basis unknown;
Alternative titles and symbols : CHDS1;
Description : Coronary heart disease is a complex multifactorial disorder for which several loci
have been identified. CHDS1 represents a locus on chromosome 16pter-p13; CHDS2 (608316),
on 2q21.1-q22; CHDS3 (300464), on Xq23-q26; CHDS4 (608318), on 14q32, and CHDS9 (612030)
on 8p22. CHDS5 (608901) represents susceptibility associated with single-nucleotide
polymorphism (SNP) in the KALRN gene (604605), on 3q13. CHDS6 (614466) is associated
with a polymorphism in the promoter region of the MMP3 gene (185250), and CHDS7 (610938)
represents susceptibility correlated with a common haplotype in the CD36 gene (173510)
and high free fatty acid levels. CHDS8 (611139) is associated with SNP variation on
9p21.;
Prefixed ID : %607339;
Origin ID : 607339;
UMLS CUI : C1846418;
DO Cross reference
- Genes related to phenotype
- Semantic type(s)
