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Resource Name
RRID:SCR_006427 RRID Copied      
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Clinical Genomic Database (RRID:SCR_006427)
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The RRID (nlx_152872) is not the primary RRID. It is an alternate RRID or alternate ID.

Resource Information

URL: http://research.nhgri.nih.gov/CGD/

Proper Citation: Clinical Genomic Database (RRID:SCR_006427)

Description: Manually curated database of all conditions with known genetic causes, focusing on medically significant genetic data with available interventions. Includes gene symbol, conditions, allelic conditions, inheritance, age in which interventions are indicated, clinical categorization, and general description of interventions/rationale. Contents are intended to describe types of interventions that might be considered. Includes only single gene alterations and does not include genetic associations or susceptibility factors related to more complex diseases.

Abbreviations: CGD

Synonyms: Clinical Genomics Database

Resource Type: data or information resource, database

Defining Citation: PMID:23696674

Keywords: genomic sequencing, genome, clinical, pediatric, adult human, young human, genomic medicine, whole-genome sequencing, gene, organ system, intervention, gene symbol, condition, allelic condition, clinical categorization, manifestation, inheritance, age group, genetic variant, pathogenic mutation

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