FIDD

Contains data on the frequency of inherited human disorders. FIDD is useful in a clinical context, in medical research, for epidemiological studies, and for the planning of genetic services. It can be queried by the body system mainly affected by the disorder, the name of the disease or condition, its Online Mendelian Inheritance in Man (OMIM) number or the population surveyed. The database covers information of over 200 conditions.

FIDD specifications

Dataset

Information

Unique identifier	OMICS_22314
Name	FIDD
Alternative name	Frequency of Inherited Disorders Database
Restrictions to use	None
Community driven	No
Data access	Browse
User data submission	Not allowed
Maintained	Yes

Maintainer

Layla Al-Jader

Additional information

https://medicapps.cardiff.ac.uk/fidd/about.aspx https://medicapps.cardiff.ac.uk/fidd/help.aspx

Publication for Frequency of Inherited Disorders Database

The Frequency of Inherited Disorders Database.

2001 Hum Genet

PMID: 11214911

FIDD institution(s)

Department of Epidemiology and Public Health, University of Wales College of Medicine, Heath Park, Cardiff, UK; Institute of Medical Genetics, University of Wales College of Medicine, Cardiff, UK

FIDD reviews

Be the first to review FIDD