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The Mendelian Inheritance in Man project is a database that catalogues all the known [diseases with a genetic component, and - when possible - links them to the relevant genes in the human genome. It is available as a book titled Mendelian Inheritance in Man (MIM), which is currently in its 12th edition.
OMIM™ and Online Mendelian Inheritance in Man™ are trademarks of the Johns Hopkins University.
The information in this database is collected and processed under the leadership of Dr. Victor A. McKusick at Johns Hopkins University, assisted by a team of science writers and editors. Relevant articles are identified, discussed and written up in the relevant entries in the MIM database
The MIM codeEdit
Every disease and gene is assigned a six digit number of which the first number classifies the method of inheritance.
|First Digit||Range of MIM codes||Method of inheritance|
|1||100000-199999||Autosomal loci or phenotypes (created before May 15, 1994)|
|2||200000-299999||Autosomal loci or phenotypes (created before May 15, 1994)|
|3||300000-399999||X-linked loci or phenotypes|
|4||400000-499999||Y-linked loci or phenotypes|
|5||500000-599999||Mitochondrial loci or phenotypes|
|6||600000-||Autosomal loci or phenotypes (created after May 15, 1994)|
- Table from the OMIM FAQ
- McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders. Baltimore, MD: The Johns Hopkins University Press, 1998. ISBN 0-8018-5742-2.
- Online Mendelian Inheritance in Man (to search OMIM)
|Databases supported by Bioinformatic Harvester|
| UniProt | SOURCE | SMART | SOSUI | PSORT | HomoloGene | GFP-cDNA | IPI | OMIM |
NCBI-BLAST | Genome-Browser | Ensembl | RZPD | STRING | iHOP | Entrez
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- fr:Héritage mendélien chez l'Homme
- hu:Mendeli öröklődés emberben adatbázis
- pt:Online Mendelian Inheritance in Man
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