Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

McKusick's Online Mendelian Inheritance in Man (OMIM).

Nucleic acids research - 1 Jan 2009

Amberger Joanna, Bocchini Carol A, Scott Alan F, Hamosh Ada

Abstract excerpt

McKusick's Online Mendelian Inheritance in Man (OMIM; http://www.ncbi.nlm.nih.gov/omim), a knowledgebase of human genes and phenotypes, was originally published as a book, Mendelian Inheritance in Man, in 1966. The content of OMIM is derived exclusively from the published biomedical literature and is updated daily. It currently contains 18,961 full-text entries describing phenotypes and genes. To date, 2239 genes...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Databases, Genetic
Share to Disease
Share to Genes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Mutation

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 18842627
DOI: 10.1093/nar/gkn665
PMCID: PMC2686440

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

McKusick's Online Mendelian Inheritance in Man (OMIM).PMID 18842627Read ↗

Online Mendelian Inheritance in Man (OMIM).Semantic proximity Read ↗

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.Semantic proximity Read ↗

Searching Online Mendelian Inheritance in Man (OMIM) for information on genetic loci involved in human disease.Semantic proximity Read ↗

OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders.Semantic proximity Read ↗

Searching Online Mendelian Inheritance in Man (OMIM) for information for genetic loci involved in human disease.Semantic proximity Read ↗

Searching Online Mendelian Inheritance in Man (OMIM): A Knowledgebase of Human Genes and Genetic Phenotypes.Semantic proximity Read ↗

Mendelian Inheritance in Man and its online version, OMIM.Semantic proximity Read ↗

Using Online Mendelian Inheritance in Man in low- and middle-income countries.Semantic proximity Read ↗

A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®).Semantic proximity Read ↗

OMIM.org: leveraging knowledge across phenotype–gene relationshipsSemantic proximity Read ↗

Contribution of Mendelian disorders to common chronic disease: opportunities for recognition, intervention, and prevention.Semantic proximity Read ↗

Disease genetics: a Mendelian code for complex disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.