data.omim.orgOMIM - Online Mendelian Inheritance in Man

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Data.omim.org is a subdomain of omim.org, which was created on 2001-10-03,making it 22 years ago. It has several subdomains, such as genescout.omim.org mirror.omim.org , among others.

Description:Explore a comprehensive compendium of human genes and genetic phenotypes with OMIM, updated daily and freely available online....

Keywords:Mendelian Inheritance in Man, OMIM, Mendelian diseases, Mendelian disorders, genetic research...

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WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME ...
https://data.omim.org/clinicalSynopsis/602418
HATIPOGLU IMMUNODEFICIENCY SYNDROME; HATIS ...
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Entry - 613601 - EARLY REPOLARIZATION ASSOCIATED ...
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MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6 ...
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MITOCHONDRIAL RIBOSOMAL PROTEIN S17; MRPS17 ...
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Entry - %607644 - CANDIDIASIS, FAMILIAL, 3; CANDF3
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Clinical Synopsis - ADAMS-OLIVER SYNDROME 5; AOS5
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Clinical Synopsis - #619764 - CHARCOT-MARIE-TOOTH ...
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Toggle navigation About Statistics Update List Entry Statistics Phenotype-Gene Statistics Pace of Gene Discovery Graph Downloads Register for Downloads Register for API Access Contact Us MIMmatch Donate Donate! Donors Help Frequently Asked Questions (FAQs) Search Help Linking Help API Help External Links Use Agreement Copyright OMIM ® An Online Catalog of Human Genes and Genetic Disorders Updated May 10th, 2024 OMIM search Advanced Search : OMIM , Clinical Synopses , Gene Map Need help? : Example Searches , OMIM Search Help , OMIM Video Tutorials Mirror site : https://mirror.omim.org OMIM is supported by a grant from NHGRI, licensing fees, and generous contributions from people like you . Make a donation! NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions. OMIM ® and Online Mendelian Inheritance in Man ® are registered trademarks of the Johns Hopkins University. Copyright ® 1966-2024 Johns Hopkins University. NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions. OMIM ® and Online Mendelian Inheritance in Man ® are registered trademarks of the Johns Hopkins University. Copyright ® 1966-2024 Johns Hopkins University. Printed: May 14, 2024 × OMIM Donation: Dear OMIM User, To ensure long-term funding for the OMIM project, we have diversified our revenue stream. We are determined to keep this website freely accessible. Unfortunately, it is not free to produce. Expert curators review the literature and organize it to facilitate your work. Over 90% of the OMIM’s operating expenses go to salary support for MD and PhD science writers and biocurators. Please join your colleagues by making a donation now and again in the future. Donations are an important component of our efforts to ensure long-term funding to provide you the information that you need at your fingertips. Thank you in advance for your generous support, Ada Hamosh, MD, MPH Scientific Director, OMIM Donate To...

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