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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:pervasive developmental disorder
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Accession:DOID:0060040 term browser browse the term
Definition:A developmental disorder of mental health that refers to a group of five disorders characterized by impairments in socialization and communication, as well as restricted interests and repetitive behaviors. (DO)
Synonyms:exact_synonym: pervasive child development disorders;   pervasive development disorder;   pervasive development disorders
 primary_id: MESH:D002659
 alt_id: DOID:9000537
 xref: ICD9CM:299.80;   NCI:C97179



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Your selection has 2432 annotated objects. The maximum number of objects that can be shown is 2000. The list is too large to display.

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  • Term paths to the root
    Path 1
    Term Annotations click to browse term
      disease 19099
        Developmental Disease 14598
          Neurodevelopmental Disorders 6946
            pervasive developmental disorder 2439
              Infantile Hyperuricemia with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase 0
              Rett syndrome + 38
              autism spectrum disorder + 2421
              childhood disintegrative disease 0
    Path 2
    Term Annotations click to browse term
      disease 19099
        disease of anatomical entity 18440
          nervous system disease 14334
            central nervous system disease 12604
              brain disease 11833
                disease of mental health 8425
                  developmental disorder of mental health 5646
                    pervasive developmental disorder 2439
                      Infantile Hyperuricemia with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase 0
                      Rett syndrome + 38
                      autism spectrum disorder + 2421
                      childhood disintegrative disease 0
    paths to the root