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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-linked central diabetes insipidus
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Accession:DOID:0081059 term browser browse the term
Definition:A central diabetes insipidus that has_material_basis_in X-linked inheritance. (DO)
Synonyms:exact_synonym: X-linked neurohypophyseal diabetes insipidus
 primary_id: MIM:304900
 xref: ORDO:30925


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19099
    Developmental Disease 14598
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 13610
        genetic disease 13271
          monogenic disease 10820
            X-linked monogenic disease 1452
              X-linked central diabetes insipidus 0
Path 2
Term Annotations click to browse term
  disease 19099
    disease of anatomical entity 18440
      nervous system disease 14333
        central nervous system disease 12605
          brain disease 11834
            hypothalamic disease 507
              pituitary gland disease 274
                diabetes insipidus 28
                  central diabetes insipidus 1
                    X-linked central diabetes insipidus 0
paths to the root