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This is a static copy of data that is exported from IATE on an occasional basis. It should not be assumed that information provided about an entry here will always correspond to the current version of the entry in IATE. That current version can be checked by clicking on the link on the upper right hand side of each entry. More information »

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  1. SOCIAL QUESTIONS|health|illness · SOCIAL QUESTIONS|health|medical science · EDUCATION AND COMMUNICATIONS|information technology and data processing
    Oidhreacht Mheindeileach an Duine ar líne Reference Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    OMIM | Online Mendelian Inheritance in Man
    en
    Definition comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily Reference "OMIM® - Online Mendelian Inheritance in Man®, http://www.omim.org/about [17.6.2013]"
    Comment 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. This database was initiated in the early 1960s by Dr. Victor A. McKusick as a catalog of mendelian traits and disorders, entitled Mendelian Inheritance in Man (MIM). Twelve book editions of MIM were published between 1966 and 1998. The online version, OMIM, was created in 1985 by a collaboration between the National Library of Medicine and the William H. Welch Medical Library at Johns Hopkins. It was made generally available on the internet starting in 1987. In 1995, OMIM was developed for the World Wide Web by NCBI, the National Center for Biotechnology Information. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, under the direction of Dr. Ada Hamosh.