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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 Inactivation, Familial Skewed, 2
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Accession:DOID:9003038 term browser browse the term
Synonyms:exact_synonym: SXI2
 primary_id: MESH:C564572
 alt_id: OMIM:300179


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21126
    Developmental Disease 18447
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18306
        genetic disease 18250
          monogenic disease 10365
            X-linked monogenic disease 1366
              X Inactivation, Familial Skewed, 2 0
paths to the root