OMIM is a comprehensive, authoritative, and timely compendium of human genes and genetic phenotypes. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes. OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources.
Online Mendelian Inheritance in Man (OMIM)
2013-06-17T16:10:59-04:00By Ollibean|Categories: General, Medical, Resources|Tags: all disabilities, Deaf Hard of Hearing, developmental disabilities, DOE, hearing impairment, inclusion, muscular dystrophies, OMIM, phenotype, rare or undiagnosed disorders, resources, spinal muscular atrophyall disabilities|0 Comments
About the Author: Ollibean
Ollibean is a dynamic community of parents, families and advocates in the disability community working together for a more socially just, accessible and inclusive world.
This site uses Akismet to reduce spam. Learn how your comment data is processed.