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Term:dilated cardiomyopathy 1H
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Accession:DOID:0110429 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 2q14-q22. (DO)
Synonyms:exact_synonym: CMD1H;   dilated cardiomyopathy with conduction defect
 primary_id: MESH:C536277
 alt_id: OMIM:604288;   RDO:0001793
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dilated cardiomyopathy 1H term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Adrb3 adrenoceptor beta 3 JBrowse link 16 69,003,541 69,006,632 RGD:5684357
G Aifm1 apoptosis inducing factor, mitochondria associated 1 JBrowse link X 135,304,063 135,343,062 RGD:10053590
G Cyp11b3 cytochrome P450, family 11, subfamily b, polypeptide 3 JBrowse link 7 116,155,928 116,161,781 RGD:1576426
G Lmna lamin A/C JBrowse link 2 187,842,884 187,863,552 RGD:8554872
G Mybpc3 myosin binding protein C3 JBrowse link 3 79,940,509 79,958,731 RGD:8554872
G RT1-Ba RT1 class II, locus Ba JBrowse link 20 4,066,133 4,070,726 RGD:5147650
G RT1-Bb RT1 class II, locus Bb JBrowse link 20 4,043,726 4,049,367 RGD:5147650
G Slc25a4 solute carrier family 25 member 4 JBrowse link 16 49,266,903 49,270,698 RGD:9681470
G Tnf tumor necrosis factor JBrowse link 20 5,189,382 5,192,000 RGD:7401234
G Trpc5 transient receptor potential cation channel, subfamily C, member 5 JBrowse link X 115,624,670 115,908,248 RGD:10044019

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  disease 16022
    Developmental Diseases 9336
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8164
        genetic disease 7688
          monogenic disease 5446
            dilated cardiomyopathy 1H 10
Path 2
Term Annotations click to browse term
  disease 16022
    disease of anatomical entity 15275
      cardiovascular system disease 4377
        heart disease 2600
          cardiomyopathy 1043
            intrinsic cardiomyopathy 707
              dilated cardiomyopathy 286
                dilated cardiomyopathy 1H 10
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.