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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 type 4B3
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Accession:DOID:0110194 term browser browse the term
Definition:A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SBF1 gene on chromosome 22q. (DO)
Synonyms:exact_synonym: CMT4B3;   SBF1-RELATED CONDITION
 primary_id: OMIM:615284
 xref: NCI:C190871;   ORDO:363981


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Charcot-Marie-Tooth disease type 4B3 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G PPP6R2 protein phosphatase 6 regulatory subunit 2 ISO ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 4B3 ClinVar PMID:23749797 PMID:33987933 NCBI chr19:32,824,732...32,917,356
Ensembl chr19:32,866,039...32,916,534
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G SBF1 SET binding factor 1 ISO ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 4B3 | ClinVar Annotator: match by term: SBF1-related condition OMIM
ClinVar
PMID:9536098 PMID:16199547 PMID:17576681 PMID:21210780 PMID:23749797 More... NCBI chr19:32,919,029...32,945,333
Ensembl chr19:32,919,341...32,938,690
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15274
    disease of anatomical entity 14909
      musculoskeletal system disease 7705
        neuromuscular disease 3016
          Charcot-Marie-Tooth disease 664
            Charcot-Marie-Tooth disease type 4 62
              Charcot-Marie-Tooth disease type 4B3 2
Path 2
Term Annotations click to browse term
  disease 15274
    disease of anatomical entity 14909
      nervous system disease 13001
        central nervous system disease 11635
          neurodegenerative disease 4682
            Nervous System Heredodegenerative Disorders 3226
              motor peripheral neuropathy 1207
                Charcot-Marie-Tooth disease 664
                  Charcot-Marie-Tooth disease type 4 62
                    Charcot-Marie-Tooth disease type 4B3 2
paths to the root