Description | Online Mendelian Inheritance in Man is a database of human phenotypes (e.g. diseases) with known genetic basis. Each entry in OMIM summarizes the current state of knowledge about a gene or phenotype, with a focus on inheritance. Genotype/phenotype associations are summarized in a document called the Morbid Map, which lists phenotypes alongside the genes that have mutations known to play a role in manifestation of the phenotype. |
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Acronym | OMIM |
External Link | http://www.omim.org/ |
Dataset | Description | Category | Attribute | Views |
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Gene-Disease Associations | Disease- or phenotype-causing gene mutations for heritable human diseases or phenotypes curated from biomedical publications | disease or phenotype associations | phenotype | 19662 |