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1 de ene. de 2002 · The content, Mendelian Inheritance in Man, has been computerized since 1964 and periodically published, first in 1966 and the twelfth edition in 1998 . The print editions began as ‘catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes’; since 1992 the subtitle of MIM has been ‘catalogs of human genes and genetic disorders’.
1 de ene. de 2002 · OMIM has been generally available online since 1987, first from Johns Hopkins and since 1995 from the NCBI. The content, Mendelian Inheritance in Man, has been computerized since 1964 and periodically published, first in 1966 and the twelfth edition in 1998 .
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.
Online Mendelian Inheritance in Man (OMIM) ist eine Datenbank, in der Gene des Menschen und deren Mutationen erfasst sind. Erbliche Erkrankungen sind dadurch sehr einfach identifizierbar. Die Datenbank enthält außerdem Informationen über klinische Symptome, Erbgang, Molekulargenetik und wissenschaftliche Publikationen zu diesem Thema.
Hace 5 días · 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.
1 McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. PMID: 18842627 PMCID: PMC2686440
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.
