OMIM is a comprehensive, authoritative database that features catalogs of autosomal dominant, autosomal recessive, x-linked, y-linked, and mitochondrial phenotypes. Includes information on human genes and genetic disorders. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes.
Alternate title
Online Mendelian inheritance in man (OMIM)
OMIM - NCBI
OMIM - Online Mendelian Inheritance in Man
Alumni
Off
link string
http://www.ncbi.nlm.nih.gov/omim
MMS_id
991003929209703851
subject
primo link string
https://tufts.primo.exlibrisgroup.com/discovery/search?query=any,contains,991003929209703851&tab=Everything&search_scope=MyInst_and_CI&vid=01TUN_INST:01TUN&lang=en&offset=0
tracked
On