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ONTOLOGY REPORT - ANNOTATIONS


Term:Charcot-Marie-Tooth Disease and Deafness
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Accession:DOID:9000259 term browser browse the term
Synonyms:exact_synonym: Deafness with Charcot-Marie-Tooth Disease;   Hereditary Motor and Sensory Neuropathy with Deafness, Mental Retardation, and Absent Sensory Large Myelinated Fibers
 primary_id: MESH:C538078
 alt_id: OMIM:214370;   RDO:0004011
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Charcot-Marie-Tooth Disease and Deafness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pmp22 peripheral myelin protein 22 JBrowse link 10 49,538,588 49,568,583 RGD:8554872
Charcot-Marie-Tooth disease type 1E term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pmp22 peripheral myelin protein 22 JBrowse link 10 49,538,588 49,568,583 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14926
    sensory system disease 4270
      auditory system disease 668
        inner ear disease 475
          sensorineural hearing loss 439
            Charcot-Marie-Tooth Disease and Deafness 1
              Charcot-Marie-Tooth disease type 1E 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14096
      nervous system disease 9148
        sensory system disease 4270
          Otorhinolaryngologic Diseases 1044
            auditory system disease 668
              Hearing Disorders 554
                Hearing Loss 550
                  sensorineural hearing loss 439
                    Charcot-Marie-Tooth Disease and Deafness 1
                      Charcot-Marie-Tooth disease type 1E 1
paths to the root

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