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ONTOLOGY REPORT - ANNOTATIONS


Term:osteogenesis imperfecta type 17
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Accession:DOID:0110338 term browser browse the term
Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the SPARC gene on chromosome 5q33. (DO)
Synonyms:exact_synonym: OI17;   osteogenesis imperfecta type XVII
 primary_id: OMIM:616507
 alt_id: RDO:9001508
For additional species annotation, visit the Alliance of Genome Resources.


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osteogenesis imperfecta type 17 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sparc secreted protein acidic and cysteine rich JBrowse link 10 40,742,390 40,764,232 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15639
    Developmental Diseases 8774
      bone development disease 1001
        osteochondrodysplasia 410
          osteogenesis imperfecta 36
            osteogenesis imperfecta type 17 1
Path 2
Term Annotations click to browse term
  disease 15639
    disease of anatomical entity 14969
      Skin and Connective Tissue Diseases 4236
        connective tissue disease 2786
          bone disease 2238
            bone development disease 1001
              osteochondrodysplasia 410
                osteogenesis imperfecta 36
                  osteogenesis imperfecta type 17 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.