Online Mendelian Inheritance in Man (OMIM) -- a knowledgebase of human genes and genetic disorders

What you can do:
Search the catalog of human genes and genetic disorders.
Highlights:
  • OMIMTM is a comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
  • Each OMIM entry has a full-text summary of a genetically determined phenotype and/or gene and has numerous links to other genetic databases such as DNA and protein sequence, PubMed references, general and locus-specific mutation databases, HUGO nomenclature, MapViewer, GeneTests, patient support groups and many others.
  • OMIM is an easy and straightforward portal to the burgeoning information in human genetics.
Keywords:
  • human genes
  • human genetics
  • human genetic diseases
  • human disease genes
  • human genetic disorders
Literature & Tutorials:
PubMed Link: OMIM
This record last updated: 05-03-2005
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