Abnormality of coagulation

0001928

Normal Case/Contol

GWAS of 0001928

Sibling Case/Control

No sibling GWAS available 0001928

Statistics

Case Control
11711 448483

Phenotype Definition

An abnormality of the process of blood coagulation. That is, altered ability or inability of the blood to clot. [HPO:probinson]


Top SNP Information

Associated Diseases

ID Name Top Correlation
ICD: D682 Hereditary deficiency of other clotting factors 7/20
ICD: D685 Primary Thrombophilia 7/20
ICD: D688 Other specified coagulation defects 7/20
ICD: K800 Calculus of gallbladder with acute cholecystitis 4/20