Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   


RGD uses the Human Disease Ontology (DO, 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:dilated cardiomyopathy 1K
go back to main search page
Accession:DOID:0110437 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 6q12-q16. (DO)
Synonyms:exact_synonym: CMD1K
 primary_id: MESH:C565320
 alt_id: OMIM:605582
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18837
    Developmental Diseases 12132
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9981
        genetic disease 9460
          monogenic disease 6898
            dilated cardiomyopathy 1K 0
Path 2
Term Annotations click to browse term
  disease 18837
    disease of anatomical entity 17323
      cardiovascular system disease 3913
        heart disease 2780
          cardiomyopathy 1177
            intrinsic cardiomyopathy 812
              dilated cardiomyopathy 337
                dilated cardiomyopathy 1K 0
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.