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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 recessive intermediate C
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Accession:DOID:0110198 term browser browse the term
Definition:A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous or compound heterozygous mutation in the PLEKHG5 gene on chromosome 1p36. (DO)
Synonyms:exact_synonym: CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE C;   CMTRIC;   RI-CMT type C;   RI-CMTC;   autosomal recessive intermediate Charcot-Marie-Tooth disease type C
 primary_id: OMIM:615376
 alt_id: RDO:9000924
 xref: ORDO:369867
For additional species annotation, visit the Alliance of Genome Resources.


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Charcot-Marie-Tooth disease recessive intermediate C term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Plekhg5 pleckstrin homology and RhoGEF domain containing G5 ISO ClinVar Annotator: match by OMIM:615376
ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, recessive intermediate c
OMIM
ClinVar
PMID:23777631 PMID:23844677 PMID:28492532 NCBI chr 5:169,244,778...169,288,310
Ensembl chr 5:169,244,778...169,288,309
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16085
    disease of anatomical entity 15340
      musculoskeletal system disease 5799
        neuromuscular disease 1802
          Charcot-Marie-Tooth disease 325
            Charcot-Marie-Tooth disease intermediate type 189
              Charcot-Marie-Tooth disease recessive intermediate C 1
Path 2
Term Annotations click to browse term
  disease 16085
    disease of anatomical entity 15340
      nervous system disease 10967
        central nervous system disease 9119
          neurodegenerative disease 3235
            Nervous System Heredodegenerative Disorders 1952
              motor peripheral neuropathy 536
                Charcot-Marie-Tooth disease 325
                  Charcot-Marie-Tooth disease intermediate type 189
                    Charcot-Marie-Tooth disease recessive intermediate C 1
paths to the root