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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Charcot-Marie-Tooth disease axonal type 2CC
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Accession:DOID:0110180 term browser browse the term
Definition:An autosomal dominant peripheral neuropathy that predominantly affects the lower limbs, resulting in muscle weakness and atrophy and gait impairment. (OMIM)
Synonyms:exact_synonym: CMT2CC;   Charcot-Marie-Tooth neuropathy, type 2CC
 primary_id: OMIM:616924
 alt_id: RDO:9000361
For additional species annotation, visit the Alliance of Genome Resources.


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Charcot-Marie-Tooth disease axonal type 2CC term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Nefh neurofilament heavy chain ISO ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC
ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, axonal, type 2CC
ClinVar
OMIM
PMID:25741868 PMID:27040688 NCBI chr14:79,830,362...79,840,347
Ensembl chr14:79,830,362...79,840,351
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17207
    disease of anatomical entity 16553
      musculoskeletal system disease 6418
        neuromuscular disease 1835
          Charcot-Marie-Tooth disease 326
            Charcot-Marie-Tooth disease type 2 63
              Charcot-Marie-Tooth disease axonal type 2CC 1
Path 2
Term Annotations click to browse term
  disease 17207
    disease of anatomical entity 16553
      nervous system disease 12101
        central nervous system disease 10378
          neurodegenerative disease 3507
            Nervous System Heredodegenerative Disorders 2118
              motor peripheral neuropathy 497
                Charcot-Marie-Tooth disease 326
                  Charcot-Marie-Tooth disease type 2 63
                    Charcot-Marie-Tooth disease axonal type 2CC 1
paths to the root