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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:Brachydactyly, Type E
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Accession:DOID:9006432 term browser browse the term
Synonyms:exact_synonym: BDE
 primary_id: MESH:C566194


show annotations for term's descendants           Sort by:
Brachydactyly, Type E term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G HDAC4 histone deacetylase 4 ISO CTD Direct Evidence: marker/mechanism CTD PMID:24715439 NCBI chr15:138,378,237...138,657,266
Ensembl chr15:138,381,635...138,614,301 		JBrowse link
G HOXD13 homeobox D13 ISO ClinVar Annotator: match by term: Brachydactyly type E ClinVar PMID:12620993 PMID:12649808 PMID:16314414 NCBI chr15:81,893,997...81,897,965
Ensembl chr15:81,893,972...81,896,944 		JBrowse link
brachydactyly type E1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G HDAC4 histone deacetylase 4 ISO ClinVar Annotator: match by term: Brachydactyly syndrome type E ClinVar PMID:10958686 PMID:11486037 PMID:25741868 PMID:33537682 NCBI chr15:138,378,237...138,657,266
Ensembl chr15:138,381,635...138,614,301 		JBrowse link
G HOXD13 homeobox D13 ISO ClinVar Annotator: match by term: Brachydactyly type E1 OMIM
ClinVar		 PMID:12414828 PMID:22233338 PMID:25741868 PMID:28492532 NCBI chr15:81,893,997...81,897,965
Ensembl chr15:81,893,972...81,896,944 		JBrowse link
brachydactyly type E2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G PTHLH parathyroid hormone like hormone ISO ClinVar Annotator: match by term: Brachydactyly type E2 OMIM
ClinVar		 PMID:20170896 PMID:25741868 PMID:25801215 PMID:26763883 PMID:29947179 More... NCBI chr 5:45,750,968...45,763,421
Ensembl chr 5:45,751,292...45,763,415 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15346
    Developmental Disease 13353
      bone development disease 2311
        dysostosis 610
          brachydactyly 34
            Brachydactyly, Type E 3
              Brachydactyly Type E, with Atrial Septal Defect, Type II 0
              Exostoses with Anetodermia and Brachydactyly Type E 0
              brachydactyly type E1 2
              brachydactyly type E2 1
Path 2
Term Annotations click to browse term
  disease 15346
    disease of anatomical entity 15037
      Skin and Connective Tissue Diseases 6983
        connective tissue disease 5413
          bone disease 3911
            bone development disease 2311
              dysostosis 610
                brachydactyly 34
                  Brachydactyly, Type E 3
                    Brachydactyly Type E, with Atrial Septal Defect, Type II 0
                    Exostoses with Anetodermia and Brachydactyly Type E 0
                    brachydactyly type E1 2
                    brachydactyly type E2 1
paths to the root