home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
  HUM-MOLGEN -> Genetic News | search  
 

New Online Syndrome Resource: Multiple Congenital Anomaly/Mental Retardation

 
  December, 22 1999 11:00
your information resource in human molecular genetics
 
     
http://www.nlm.nih.gov/mesh/jablonski/syndrome_title.html

The National Library of Medicine is pleased to announce a new Web-based resource to help health practitioners, librarians and others identify syndromes in which multiple congenital anomalies are associated with mental retardation. Multiple Congenital Anomaly/Mental Retardation has been developed by Stanley Jablonski in collaboration with the Office of Computer and Communications Systems (OCCS) and the Medical Subject Headings Section.

At the present time the system includes structured descriptions of approximately 700 out of the 1600-2000 syndromes of congenital abnormalities known to be associated with mental retardation. Additional entries will be added in the future. There is provision for knowledgeable individuals to submit additional entries for eventual inclusion. As a unique aspect of the scope, this system encompasses chromosomal aberrations and x-linked mental retardation characteristics, some of which are not routinely designated in the literature as syndromes, but possess sufficient syndromic characteristics. Information about each syndrome includes synonyms, personalia, OMIM entries, Unified Medical Subject Headings (UMLS) entries, and MeSH terms. The interface has been based on the logic and format of the MeSH browser, also accessible to users from the NLM Web site.


Message posted by: Frank S. Zollmann

print this article mail this article
Bookmark and Share this page (what is this?)

Social bookmarking allows users to save and categorise a personal collection of bookmarks and share them with others. This is different to using your own browser bookmarks which are available using the menus within your web browser.

Use the links below to share this article on the social bookmarking site of your choice.

Read more about social bookmarking at Wikipedia - Social Bookmarking

Latest News
Variants Associated with Pediatric Allergic Disorder

Mutations in PHF6 Found in T-Cell Leukemia

Genetic Risk Variant for Urinary Bladder Cancer

Antibody Has Therapeutic Effect on Mice with ALS

Regulating P53 Activity in Cancer Cells

Anti-RNA Therapy Counters Breast Cancer Spread

Mitochondrial DNA Diversity

The Power of RNA Sequencing

‘Pro-Ageing' Therapy for Cancer?

Niche Genetics Influence Leukaemia

Molecular Biology: Clinical Promise for RNA Interference

Chemoprevention Cocktail for Colon Cancer

more news ...

Generated by News Editor 2.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995-2016 HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.