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FIDD: The Frequency of Inherited Disorders Database

IDNBDC common database IDs, which should be written in parentheses if there are multiple titles, such as Japanese and English. NBDC00269
Database nameName of the database FIDD
Alternative nameAlternative name of the database The Frequency of Inherited Disorders Database
URLURL of the database https://medicapps.cardiff.ac.uk/fidd/
Database maintenance siteSite maintaining the database Cardiff University School of Medicine
Country/RegionCountry or region name where the database maintenance site is located United Kingdom
Database descriptionDatabase descirption FIDD (Frequency of Inherited Disorders Database) belongs to the Institute of Medical genetics at the Cardiff University School of Medicine. This database provides information about the frequency of human Mendelian disorders and how widespread these diseases occur. The site was created for the purpose of use in medical research and the study of epidemiological occurrences in order to establish genetic service delivery. FIDD contains a total of 1580 records of human genetic disorders listed in 14 groups related to the organ, body system or biological function affected. There are 280 disorders that are covered, and of them 109 are autosomal dominant, 136 are autosomal recessive and 35 are X-linked. There are 969 articles, which have been published in 215 journals, a variety of 119 books, 9 doctoral theses and 22 reports that were scrutinized to obtain the information available in this repository. The results reveal 24 cardiac disorders, 34 endocrine disorders and 44 disorders of the eye. It also contains information on 31 disorders of the gastrointestinal system, 353 hematological anomalies and 22 disorders causing mental handicaps. A total of 234 disorders of the metabolic system and 588 affecting the neurological and neuromuscular systems are described, and 3 psychiatric disorders, 35 of the renal system and 25 respiratory disorders are also covered. The information content also include 72 disorders of the skeletal and craniofacial group, 46 skin anomalies and 69 disorders that could not be allocated to a specific body system. A keyword search option is available whereby information can be retrieved by entering the body system, disease, population or OMIM number in question.
Organism(s) coveredNCBI Taxonomy names and IDs covered by the database Homo sapiens (9606)
Tag - TargetTag to indicate targets for this database such as genome and protein
Genome/Gene
cDNA/EST
Genetic variation
Epigenetics
DNA
RNA
Protein
Carbohydrate
Lipid
Metabolite
Chemical compound
Drug
Cell/Organelle
Organism
Health/Disease
Tag - Information typeTag to indicate information types for this database such as sequence and structure
Phenotype
Bioresource
Method
Ontology/Terminology/Nomenclature
Environment
Sequence
3D structure
Chemical structure
Expression
Localization
Geographic Distribution
Interaction/Pathway
Taxonomy
Classification
Image/Movie
Bibliography/Documents
Portal
Repository
Reference(s) - PubMed ID/DOIPubMed IDs/DOI for papers related to the database
Language(s)Languages in which the contents of the database are displayed English
Operational statusOperational status for the database Active
Link(s) to Downloadable dataLinks to downloadable data
Link(s) to MetaData of downloadable dataLinks to metadata of downloadable data
Link(s) to Terms of useLinks to terms of use of downloadable data
Link(s) to "How to use"
Contact information of database
Link(s) to API / SPARQL endpoint
Link to LSDB ArchiveLink to LSDB Archive
Link to MEDALS Database listLink to MEDALS Database list
Link to TogoTVLink to TogoTV
Link to FAIRsharingLink to FAIRsharing
Similar databasesDatabases that are similar to this database.
Record maintainerRecord maintainer Integbio Database Catalog
Record sourceOrganization that originally created the record
Date of creation of this recordDate of creation of this English record 2013-06-17
Last update date of this recordLast update date of this English record 2016-03-14
Record license Creative Commons CC0 license