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Hace 4 días · OMIM. OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. 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. Its official home is omim.org.
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. Die Website erlaubt einfache Suche nach Begriffen, aber ...
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 ...
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 ...
13 de may. de 2018 · Definition. Online Mendelian Inheritance in Man®, kurz OMIM®, ist eine medizinische Online-Datenbank menschlicher Gene sowie genetischer Phänotypen und Erkrankungen. Der Katalog enthält zudem Informationen zu den jeweiligen Erbgängen, entsprechende DNA-Sequenzen und klinische Symptome der Erkrankungen.
13 de ago. de 2016 · OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders. [PMID: 25428349]
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 ...
