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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Abnormalities, Drug-Induced
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Accession:DOID:9007828 term browser browse the term
Definition:Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment.
Synonyms:exact_synonym: Drug-Induced Abnormality
 primary_id: MESH:D000014;   RDO:0000716
For additional species annotation, visit the Alliance of Genome Resources.



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Abnormalities, Drug-Induced term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G CAT catalase ISO CTD Direct Evidence: therapeutic CTD PMID:21252394 PMID:26074427 NCBI chr18:33,383,005...33,422,447
Ensembl chr18:33,383,005...33,422,447
JBrowse link
G CRBN cereblon ISO CTD Direct Evidence: marker/mechanism CTD PMID:27751757 NCBI chr20:14,240,723...14,275,617
Ensembl chr20:14,240,804...14,274,940
JBrowse link
G EPHX1 epoxide hydrolase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:2336087 NCBI chr 7:38,964,319...39,004,902
Ensembl chr 7:38,964,338...38,999,238
JBrowse link
G RHOA ras homolog family member A ISO CTD Direct Evidence: marker/mechanism CTD PMID:25783350 NCBI chr20:39,824,552...39,888,089
Ensembl chr20:39,824,575...39,887,215
JBrowse link
G WNT11 Wnt family member 11 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25783350 NCBI chr21:22,442,496...22,463,040
Ensembl chr21:22,446,051...22,463,173
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13847
    Developmental Disease 10404
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8963
        Congenital Abnormalities 5440
          Abnormalities, Drug-Induced 5
            Accutane Embryopathy 0
            Acitretin Embryopathy 0
            Fetal Hydantoin Syndrome 0
            Fetal Trimethadione Syndrome 0
            Ho Kaufman Mcalister Syndrome 0
            Isotretinoin Embryopathy Like Syndrome 0
            Warfarin Syndrome 0
            fetal valproate syndrome 0
paths to the root