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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:INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES
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Accession:DOID:9007433 term browser browse the term
Synonyms:exact_synonym: IDDSSA
 primary_id: OMIM:618453
For additional species annotation, visit the Alliance of Genome Resources.


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INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G WIPI2 WD repeat domain, phosphoinositide interacting 2 ISO OMIM NCBI chr 6:12,656,469...12,698,623
Ensembl chr 6:12,658,239...12,698,734
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13760
    Developmental Disease 10355
      Neurodevelopmental Disorders 5601
        INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES 1
Path 2
Term Annotations click to browse term
  disease 13760
    disease of anatomical entity 13412
      nervous system disease 11166
        central nervous system disease 9764
          brain disease 9170
            disease of mental health 6738
              Neurodevelopmental Disorders 5601
                INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES 1
paths to the root