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ONTOLOGY REPORT - ANNOTATIONS


Term:Charcot-Marie-Tooth disease type 1D
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Accession:DOID:0110150 term browser browse the term
Definition:A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the early growth response gene-2 (EGR2). (DO)
Synonyms:exact_synonym: CMT1D;   Charcot-Marie-Tooth Neuropathy, Type 1D;   Charcot-Marie-Tooth disease, demyelinating, Type 1D;   HMSN 1D;   HMSN ID;   HMSN1D;   HMSNID;   Hereditary motor and sensory neuropathy 1D
 primary_id: MESH:C537985
 alt_id: OMIM:607678;   RDO:0003914
 xref: ORDO:101084
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Charcot-Marie-Tooth disease type 1D term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Egr2 early growth response 2 JBrowse link 20 22,452,170 22,461,018 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15620
    disease of anatomical entity 14949
      musculoskeletal system disease 4277
        neuromuscular disease 1522
          Charcot-Marie-Tooth disease 318
            Charcot-Marie-Tooth disease type 1 12
              Charcot-Marie-Tooth disease type 1D 1
Path 2
Term Annotations click to browse term
  disease 15620
    disease of anatomical entity 14949
      nervous system disease 10219
        central nervous system disease 8096
          neurodegenerative disease 2691
            Nervous System Heredodegenerative Disorders 1718
              motor peripheral neuropathy 458
                Charcot-Marie-Tooth disease 318
                  Charcot-Marie-Tooth disease type 1 12
                    Charcot-Marie-Tooth disease type 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.