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ONTOLOGY REPORT - ANNOTATIONS


Term:Craniodiaphyseal Dysplasia, Autosomal Dominant
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Accession:DOID:9003280 term browser browse the term
Synonyms:exact_synonym: CDD
 primary_id: MESH:C567275
 alt_id: OMIM:122860;   RDO:0015391
For additional species annotation, visit the Alliance of Genome Resources.


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Craniodiaphyseal Dysplasia, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sost sclerostin JBrowse link 10 89,897,087 89,900,131 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      musculoskeletal system disease 4271
        Musculoskeletal Abnormalities 1302
          Craniofacial Abnormalities 1046
            craniodiaphyseal dysplasia 1
              Craniodiaphyseal Dysplasia, Autosomal Dominant 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      musculoskeletal system disease 4271
        connective tissue disease 2763
          bone disease 2215
            bone development disease 983
              osteochondrodysplasia 408
                osteosclerosis 44
                  craniodiaphyseal dysplasia 1
                    Craniodiaphyseal Dysplasia, Autosomal Dominant 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.