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ONTOLOGY REPORT - ANNOTATIONS


Term:Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
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Accession:DOID:9007064 term browser browse the term
Synonyms:exact_synonym: SEMD, MATN3-RELATED;   SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATN3-RELATED
 primary_id: MESH:C563869
 alt_id: OMIM:608728;   RDO:0013013
For additional species annotation, visit the Alliance of Genome Resources.


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Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Matn3 matrilin 3 JBrowse link 6 34,071,428 34,091,048 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    Developmental Diseases 8737
      bone development disease 983
        osteochondrodysplasia 408
          spondyloepimetaphyseal dysplasia 71
            Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      Skin and Connective Tissue Diseases 4211
        connective tissue disease 2763
          bone disease 2215
            bone development disease 983
              osteochondrodysplasia 408
                spondyloepimetaphyseal dysplasia 71
                  Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related 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.