Online Mendelian Inheritance in Man: Difference between revisions
Jump to navigation
Jump to search
imported>Robert Badgett No edit summary |
imported>Robert Badgett (Started OMIM Numbering) |
||
| Line 2: | Line 2: | ||
:''For use of the OMIM template, see [[Template:OMIM]]'' | :''For use of the OMIM template, see [[Template:OMIM]]'' | ||
'''Online Mendelian Inheritance in Man''' (OMIM) is an online database at the U.S. National Library of Medicine about diseases that have genetic components. According to the OMIM website, OMIM is a "catalog of human genes and genetic disorders authored and edited by Dr. Victor A. McKusick and his colleagues at Johns Hopkins and elsewhere, and developed for the World Wide Web by NCBI, the National Center for Biotechnology Information. The database contains textual information and references. It also contains copious links to [[MEDLINE]] and sequence records in the Entrez system, and links to additional related resources at NCBI and elsewhere."<ref name="titleOMIM Home">{{cite web |url=http://www.ncbi.nlm.nih.gov/sites/entrez?db=omim |title=OMIM Home |accessdate=2008-03-04 |author=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=National Library of Medicine |pages= |language= |archiveurl= |archivedate= |quote=}}</ref> | '''Online Mendelian Inheritance in Man''' (OMIM) is an online database at the U.S. National Library of Medicine about diseases that have genetic components. According to the OMIM website, OMIM is a "catalog of human genes and genetic disorders authored and edited by Dr. Victor A. McKusick and his colleagues at Johns Hopkins and elsewhere, and developed for the World Wide Web by NCBI, the National Center for Biotechnology Information. The database contains textual information and references. It also contains copious links to [[MEDLINE]] and sequence records in the Entrez system, and links to additional related resources at NCBI and elsewhere."<ref name="titleOMIM Home">{{cite web |url=http://www.ncbi.nlm.nih.gov/sites/entrez?db=omim |title=OMIM Home |accessdate=2008-03-04 |author=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=National Library of Medicine |pages= |language= |archiveurl= |archivedate= |quote=}}</ref> | ||
==OMIM Numbering== | |||
{| class="wikitable" align"center" | |||
|+ OMIM Number Prefixes<ref name="urlOMIM FAQs">{{cite web |url=http://www.ncbi.nlm.nih.gov/Omim/omimfaq.html#mim_number_symbols |title=OMIM Frequently Asked Questions (FAQs) |author=Anomymous |authorlink= |coauthors= |date=February 27, 2007 |format= |work= |publisher=National Center for Biotechnology Information |pages= |language=English |archiveurl= |archivedate= |quote= |accessdate=2009-08-29}}</ref> | |||
! Prefix!! Meaning | |||
|- | |||
| <nowiki>*</nowiki> || gene with known sequence | |||
|- | |||
| <nowiki>+</nowiki>|| gene with known sequence and phenotype | |||
|- | |||
| <nowiki># </nowiki>|| phenotype description, molecular basis known | |||
|- | |||
| <nowiki>% </nowiki>|| Mendelian phenotype or locus, molecular basis unknown | |||
|- | |||
| no prefix|| other, mainly phenotypes with suspected Mendelian basis | |||
|} | |||
==References== | ==References== | ||
Revision as of 09:08, 29 August 2009
- For use of the OMIM template, see Template:OMIM
Online Mendelian Inheritance in Man (OMIM) is an online database at the U.S. National Library of Medicine about diseases that have genetic components. According to the OMIM website, OMIM is a "catalog of human genes and genetic disorders authored and edited by Dr. Victor A. McKusick and his colleagues at Johns Hopkins and elsewhere, and developed for the World Wide Web by NCBI, the National Center for Biotechnology Information. The database contains textual information and references. It also contains copious links to MEDLINE and sequence records in the Entrez system, and links to additional related resources at NCBI and elsewhere."[1]
OMIM Numbering
| Prefix | Meaning |
|---|---|
| * | gene with known sequence |
| + | gene with known sequence and phenotype |
| # | phenotype description, molecular basis known |
| % | Mendelian phenotype or locus, molecular basis unknown |
| no prefix | other, mainly phenotypes with suspected Mendelian basis |
References
- ↑ Anonymous. OMIM Home. National Library of Medicine. Retrieved on 2008-03-04.
- ↑ Anomymous (February 27, 2007). OMIM Frequently Asked Questions (FAQs) (English). National Center for Biotechnology Information. Retrieved on 2009-08-29.