OMIM - Online Mendelian Inheritance in Man
Mendelian Inheritance in Man, OMIM, Mendelian diseases, Mendelian disorders, genetic diseases, genetic disorders, genetic disorders in humans, genetic phenotypes, phenotype and genotype, disease models, alleles, genes, dna, genetics, dna testing, gene testing, clinical synopsis, medical genetics
Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 15,000 genes. OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources.