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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
Gene Disease Database; Gene Expression Omnibus (GEO [9]): a public functional genomics data repository from the U.S. National Cancer Institute (NCI), which supports array- and sequence-based data. Tools for querying and downloading gene expression profiles are provided.
The Genetic Association Database is an archive of human genetic association studies of complex diseases. GAD is primarily focused on archiving information on common complex human disease rather than rare Mendelian disorders as found in the OMIM.
Online Mendelian Inheritance in Animals (OMIA) is an online database of genes, inherited disorders and traits in more than 550 animal species. It is modelled on, and is complementary to, Online Mendelian Inheritance in Man (OMIM).
The Entrez Global Query Cross-Database Search System is used at NCBI for all the major databases such as Nucleotide and Protein Sequences, Protein Structures, PubMed, Taxonomy, Complete Genomes, OMIM, and several others. [9] Entrez is both an indexing and retrieval system having data from various sources for biomedical research.
It has also improved the speed and sophistication of the search engine, and expanded from a gene-centric dogma to contain gene-set analyses. Version 3 of the database gathers information from more than 90 database resources based on a consolidated gene list. It has also added a suite of GeneCards tools which focus on more specific purposes.
Stubs for the Gene Wiki project are created by a bot and contain links to the following primary gene/protein databases: HUGO Gene Nomenclature Committee – official gene name; Entrez – Gene database; OMIM (Mendelian Inheritance in Man) – database that catalogues all the known diseases with a genetic component; Amigo – Gene Ontology