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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:dilated cardiomyopathy 1L
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Accession:DOID:0110436 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutations in the SGCD gene on chromosome 5q33.2-q33.3. (DO)
Synonyms:exact_synonym: CMD1L
 primary_id: MESH:C564679
 alt_id: OMIM:606685
For additional species annotation, visit the Alliance of Genome Resources.



show annotations for term's descendants           Sort by:
 
dilated cardiomyopathy 1L term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Sgcd sarcoglycan, delta ISO ClinVar Annotator: match by OMIM:606685
ClinVar Annotator: match by term: Dilated cardiomyopathy 1L
OMIM
ClinVar
PMID:8841194 PMID:10735275 PMID:10838250 PMID:10974018 PMID:14564412 More... NCBI chr10:31,346,480...32,328,364
Ensembl chr10:31,280,511...31,724,840
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17289
    Developmental Disease 10990
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9530
        genetic disease 9033
          monogenic disease 7190
            dilated cardiomyopathy 1L 1
Path 2
Term Annotations click to browse term
  disease 17289
    disease of anatomical entity 16625
      cardiovascular system disease 4526
        heart disease 2702
          cardiomyopathy 1096
            intrinsic cardiomyopathy 737
              dilated cardiomyopathy 300
                dilated cardiomyopathy 1L 1
paths to the root