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Term:Compton-North congenital myopathy
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Accession:DOID:0080101 term browser browse the term
Synonyms:exact_synonym: MYPCN
 primary_id: MESH:C567261;   RDO:0015382
 alt_id: OMIM:612540
For additional species annotation, visit the Alliance of Genome Resources.

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Compton-North congenital myopathy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cntn1 contactin 1 JBrowse link 7 133,290,606 133,588,314 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15603
    Developmental Diseases 8772
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7555
        genetic disease 7051
          congenital myasthenic syndrome 57
            Compton-North congenital myopathy 1
Path 2
Term Annotations click to browse term
  disease 15603
    disease of anatomical entity 14934
      nervous system disease 10239
        peripheral nervous system disease 2138
          neuropathy 1960
            neuromuscular disease 1530
              muscular disease 968
                muscle tissue disease 689
                  myopathy 556
                    congenital myopathy 29
                      Compton-North congenital myopathy 1
paths to the root


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