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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:copper deficiency myelopathy
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Accession:DOID:5112 term browser browse the term
Definition:A nutritional deficiency disease that is characterized by deficiency of copper, causing spastic gait and ataxia, often with anemia and neutropenia, has_symptom imbalance and jerking movements, and has_material_basis_in copper deficiency possibly due to malabsorption or excess zinc ingestion. (DO)
Synonyms:exact_synonym: Enzootic Ataxia;   Enzootic Ataxias;   human swayback;   swayback;   swayback of sheep
 primary_id: MESH:D013540
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19139
    Animal Diseases 1794
      Sheep Diseases 20
        copper deficiency myelopathy 0
Path 2
Term Annotations click to browse term
  disease 19139
    Nutritional and Metabolic Diseases 8544
      disease of metabolism 8544
        acquired metabolic disease 2544
          nutrition disease 1036
            Malnutrition 284
              nutritional deficiency disease 264
                copper deficiency myelopathy 0
paths to the root