ONTOLOGY REPORT - ANNOTATIONS


Term:dilated cardiomyopathy 1D
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Accession:DOID:0110426 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the TNNT2 gene on chromosome 1q32. (DO)
Synonyms:exact_synonym: CMD1D
 narrow_synonym: LEFT VENTRICULAR NONCOMPACTION 6;   LVNC6
 primary_id: MESH:C563306
 alt_id: OMIM:601494;   RDO:0012603
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dilated cardiomyopathy 1D term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tnnt2 troponin T2, cardiac type JBrowse link 13 52,662,974 52,680,992 RGD:7240710
RGD:8554872

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  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          dilated cardiomyopathy 1D 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      cardiovascular system disease 4065
        heart disease 2230
          cardiomyopathy 899
            intrinsic cardiomyopathy 567
              dilated cardiomyopathy 270
                dilated cardiomyopathy 1D 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.