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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


show annotations for term's descendants           Sort by:
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 29219
    Pathological Conditions, Signs and Symptoms 16554
      Pathologic Processes 10082
        Chromosome Aberrations 4266
          Sex Chromosome Aberrations 10
            X Chromosome, Monosomy Xp22 pter 0
Path 2
Term Annotations click to browse term
  disease 29219
    Pathological Conditions, Signs and Symptoms 16554
      Pathologic Processes 10082
        Chromosome Aberrations 4266
          Aneuploidy 3068
            Monosomy 2766
              Chromosome Deletion 2766
                X Chromosome, Monosomy Xp22 pter 0
paths to the root