Examples of 'orphanet' in a sentence
Meaning of "orphanet"
Orphanet is a comprehensive database dedicated to information on rare diseases and orphan drugs. It provides information about rare diseases, expert resources, and research activities in this field
Show more definitions
- A young or little orphan.
How to use "orphanet" in a sentence
Basic
Advanced
orphanet
Orphanet was born.
All our items are created on popular sites such as where orphanet dictionary.
Orphanet is a database of information on rare diseases and orphan drugs for all publics.
Microlissencephaly is listed in Orphanet database as a rare disease.
Orphanet includes links to national patient organisations in Europe.
This could find applications in automating the update process of RD databases such as Orphanet.
The Orphanet portal for rare diseases and orphan drugs.
Belgian contribution to the international Orphanet portal for rare diseases and orphan drugs.
Orphanet is a European website providing information about orphan drugs and rare diseases.
It is an official journal of Orphanet and is published by BioMed Central.
Orphanet syndrome Majeed syndrome.
LFB is a major partner of Orphanet.
The established Orphanet website is a valuable step towards achieving that goal.
The results of their study are published in Orphanet Journal of Rare Diseases.
Repertorying rare diseases information, diagnosis and treatment using existing European initiatives in particular Orphanet.
See also
Created and coordinated by Inserm, the Orphanet database contains the largest amount of epidemiological.
This was made possible through a dedicated portal, OrphanXchange, that was linked to the Orphanet database.
Orphanet is led by a consortium of around 40 countries, coordinated by the French IN-SERM team.
Few databases provide information about RDs, such as Orphanet and Orphadata.
OrphaNet rare disease patient registry and biobank searchable database ( available in 7 languages ).
A paper on the CTSR has been published in the Orphanet Journal of Rare Diseases,.
The expertise is already there, said Ana Rath, director of Orphanet.
In addition, Orphanet publishes,.
In 2008, the EU decided to store information on rare diseases in the Orphanet database.