Search results
Results From The WOW.Com Content Network
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 ...
This is a list of disorder codes in the Online Mendelian Inheritance in Man (OMIM) database. These are diseases that can be inherited via a Mendelian genetic mechanism. OMIM is one of the databases housed in the U.S. National Center for Biotechnology Information. Isolated 17,20-lyase deficiency; 202110; CYP17A1
OMIM (Online Mendelian Inheritance in Man): inherited diseases; RefSeq; 1000 Genomes Project: launched in January 2008. The genomes of more than a thousand anonymous participants from a number of different ethnic groups were analyzed and made publicly available.
Maps.me is a mobile app for Android, iOS and BlackBerry that provides offline maps using OpenStreetMap data. It was formerly known as MapsWithMe.In November 2014, it was acquired by Mail.Ru Group and became part of its My.com brand.
In genetics, a morbid map is a chart or diagram of diseases and the chromosomal location of genes the diseases are associated with. A morbid map exists as an appendix of the Online Mendelian Inheritance in Man (OMIM) knowledgebase, listing chromosomes and the genes mapped to specific sites on those chromosomes, and this format most clearly reveals the relationship between gene and phenotype.
OMI was contributed to The Open Group by Microsoft on June 28, 2012, with the goal "to remove all obstacles that stand in the way of implementing standards-based management so that every device in the world can be managed in a clear, consistent, coherent way and to nurture [and] spur a rich ecosystem of standards-based management products."
Information regarding proteins involved in human diseases is annotated and linked to Online Mendelian Inheritance in Man (OMIM) database. The National Center for Biotechnology Information provides link to HPRD through its human protein databases (e.g. Entrez Gene, RefSeq protein pertaining to genes and proteins.
page name is an optional parameter to display the OMIM page name display options is an optional parameter to set various output choices. If left blank or unused, will show the linked name in full