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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, 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.
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omim genetic genes entry number mim mendelian human phenotype phenotypes online inheritance disorders known indicates entries johns hopkins medicine man
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Online Mendelian Inheritance in Man | Data types captured | Genes, genetic disorders, phenotypic traits | 1.00 | infobox |
| Online Mendelian Inheritance in Man | Description | Catalog of all known human genes and genetic phenotypes. | 1.00 | infobox |
| Online Mendelian Inheritance in Man | Organisms | Homo sapiens | 1.00 | infobox |
| Online Mendelian Inheritance in Man | Primary citation | .mw-parser-output cite.citation{font-style:inherit;word-wrap:break-word}.mw-parser-output .citation q{quotes:"\"""\"""'""'"}.mw-parser-output .citation:target{background-color:r… | 1.00 | infobox |
| Online Mendelian Inheritance in Man | Research center | Johns Hopkins University School of Medicine | 1.00 | infobox |
| Online Mendelian Inheritance in Man | Website | http://www.omim.org/ | 1.00 | infobox |
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