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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 chr 3:93,379,872...93,412,058
Ensembl chr 3:93,379,874...93,412,058 		JBrowse link
G Crbn cereblon ISO CTD Direct Evidence: marker/mechanism CTD PMID:27751757 NCBI chr 4:138,864,910...138,885,786
Ensembl chr 4:138,866,761...138,885,556 		JBrowse link
G Ephx1 epoxide hydrolase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:2336087 NCBI chr13:99,271,390...99,300,580
Ensembl chr13:99,271,366...99,300,579 		JBrowse link
G Rhoa ras homolog family member A ISO CTD Direct Evidence: marker/mechanism CTD PMID:25783350 NCBI chr 8:117,082,440...117,116,244
Ensembl chr 8:117,106,576...117,116,167 		JBrowse link
G Wnt11 Wnt family member 11 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25783350 NCBI chr 1:163,794,136...163,813,756
Ensembl chr 1:163,797,660...163,813,756 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16123
    Developmental Diseases 9597
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8441
        Congenital Abnormalities 4761
          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