Abstract: The Online Mendelian Inheritance in Man (OMIM) database is a useful reference for human genetic diseases. By standardization of its data structure, we hereby provide a user-friendly ...

The Genomic Oligoarray and SNP Array Evaluation Tool 3.0 matches candidate genes within regions of homozygosity with a patient’s phenotype, by mining OMIM for gene entries that contain a Clinical ...

P53 description_1(OMIM: id);description_2(OMIM: id);etc ... cn_description_1(OMIM: id);cn_description_2(OMIM: id);etc ... Due to the difference of annotation ...

Abstract: Phenotypic comparison may provide crucial information for obtaining insights into molecular interactions underlying various diseases. However, few attempts have been made to systematically ...