OMIM: Online Mendelian Inheritance in Man
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| Database maintenance site: | NCBI (National Center for Biotechnology Information) |
| Country/Region: | United States |
| Database description: | OMIM is a database of human disease and genetic information and the online representation of Mendelian Inheritance in Man, a project initiated in the 1960s. The database summarizes heritable traits and provides information on both the trait and experimentally determined genetic causes. The database is manually curated by experts and can be searched by OMIM ID, gene, disease, or phenotype. |
| Organism(s) covered: | |
| Tag - Target: | Genome/Gene, Genetic variation, Health/Disease |
| Tag - Information type: | Bibliography/Documents |
| Reference(s) - PubMed ID/DOI: | PubMed ID: DOI: |
| Language(s): | English |
| Operational status: | Active |
| Link(s) to Downloadable data: | http://omim.org/downloads |
| Link(s) to Metadata of downloadable data: | http://omim.org/downloads |
| Link(s) to Terms of use: | http://omim.org/help/copyright |
| Link(s) to "How to use": | - |
| Contact information of database: | - |
| Link(s) to API / SPARQL endpoint | - |
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Link to LSDB Archive:
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Link to MEDALS Database list:
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Link to TogoTV:
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https://togotv.dbcls.jp/en/result.html?type=lecture&lang=en&page=1&query=OMIM |
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Link to FAIRsharing:
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https://fairsharing.org/biodbcore-000761 |
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Similar databases:
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FIDD Catalogue of Transmission Genetics in Arabs ostogenesis imperfecta & Ehlers-Danlos syndrome variant databases IARC TP53 Database CADgene euL1db, the European database of L1-HS retrotransposon insertions in humans Digenic diseases database VaDE |
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Record maintainer
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Integbio Database Catalog |
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Record source:
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Date of creation of this record:
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2013-06-17 |
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Last update date of this record:
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2022-01-24 |
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Record license:
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Creative Commons CC0 license |