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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:X Chromosome, Monosomy Xp22 pter
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Accession:DOID:9006157 term browser browse the term
Synonyms:exact_synonym: Deletion Xp22 pter;   Monosomy Xp22 pter
 primary_id: MESH:C536754;   RDO:0002434

GViewer not supported for the selected species.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16461
    Pathological Conditions, Signs and Symptoms 11253
      Pathologic Processes 7012
        Chromosome Aberrations 2417
          Sex Chromosome Aberrations 7
            X Chromosome, Monosomy Xp22 pter 0
Path 2
Term Annotations click to browse term
  disease 16461
    Pathological Conditions, Signs and Symptoms 11253
      Pathologic Processes 7012
        Chromosome Aberrations 2417
          Aneuploidy 1665
            Monosomy 1418
              Chromosome Deletion 1418
                X Chromosome, Monosomy Xp22 pter 0
paths to the root