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ONTOLOGY REPORT - ANNOTATIONS


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 RT1-Ba RT1 class II, locus Ba JBrowse link 20 4,066,133 4,070,726 RGD:5147650
RGD:5147795
RGD:5147858
G RT1-Bb RT1 class II, locus Bb JBrowse link 20 4,043,726 4,049,367 RGD:5147650
RGD:5147858
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 15620
    Developmental Diseases 8739
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7521
        genetic disease 7009
          monogenic disease 4562
            dilated cardiomyopathy 1H 8
Path 2
Term Annotations click to browse term
  disease 15620
    disease of anatomical entity 14949
      cardiovascular system disease 4286
        heart disease 2379
          cardiomyopathy 931
            intrinsic cardiomyopathy 603
              dilated cardiomyopathy 267
                dilated cardiomyopathy 1H 8
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.