Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.

European journal of human genetics : EJHG - 1 Mar 2014

Charoute Hicham, Nahili Halima, Abidi Omar, Gabi Khalid, Rouba Hassan, Fakiri Malika, Barakat Abdelhamid

Abstract excerpt

National and ethnic mutation databases provide comprehensive information about genetic variations reported in a population or an ethnic group. In this paper, we present the Moroccan Genetic Disease Database (MGDD), a catalogue of genetic data related to diseases identified in the Moroccan population. We used the PubMed, Web of Science and Google Scholar databases to identify available articles published until...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Databases, Genetic
Share to Genetic Diseases, Inborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Morocco

Share to Polymorphism, Genetic

Source

Open in PubMed Open full text

Identifiers

PMID: 23860041
DOI: 10.1038/ejhg.2013.151
PMCID: PMC3925278

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.PMID 23860041Read ↗

Moroccan genome project: Genomic insight into a North African populationSemantic proximity Read ↗

Genetic diseases in the Tunisian population.Semantic proximity Read ↗

Repository of mutations from Oman: The entry point to a national mutation databaseSemantic proximity Read ↗

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.Semantic proximity Read ↗

Arab genetic disease database (AGDDB): a population-specific clinical and mutation database.Semantic proximity Read ↗

Indian genetic disease database.Semantic proximity Read ↗

Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.Semantic proximity Read ↗

Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan Patients.Semantic proximity Read ↗

Common disease-associated gene variants in a Saudi Arabian populationSemantic proximity Read ↗

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.Semantic proximity Read ↗

Pakistan Genetic Mutation Database (PGMD); A centralized Pakistani mutome data source.Semantic proximity Read ↗

Searching Online Mendelian Inheritance in Man (OMIM): A Knowledgebase of Human Genes and Genetic Phenotypes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.