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Herencia Mendeliana en el Hombre. Mendelian Inheritance in Man es una base de datos de genes humanos y trastornos y rasgos genéticos, con un enfoque particular en la relación gen - fenotipo. Está disponible de forma telemática en la web de la Facultad de Medicina de la Universidad Johns Hopkins, 1 en la que se actualiza prácticamente a diario.
JHU may modify the OMIM data or OMIM.org, including, without limitation, by the removal, reduction or addition of functionality or content; and/or discontinue, temporarily or permanently access to or use of OMIM; and/or change and amend this USE AGREEMENT as provided in clause 28 below, including, without limitation, by adding terms that JHU may be required to "pass through" to User as a ...
Hace 4 días · 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.
Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship. As of 28 June 2019 [update] , approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes ; the rest represented genes , many of which were related to known phenotypes.
OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources. Entry - #166200 - OSTEOGENESIS IMPERFECTA, TYPE I; OI1 - OMIM
OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources. Entry - #152700 - SYSTEMIC LUPUS ERYTHEMATOSUS; SLE - OMIM
Welcome to OMIM ®, 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 16,000 genes.
