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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:Spondyloepimetaphyseal Dysplasia, Krakow Type
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Accession:DOID:9009268 term browser browse the term
Synonyms:exact_synonym: IMMUNOOSSEOUS DYSPLASIA, KRAKOW TYPE;   SEMDK
 primary_id: OMIM:618162
For additional species annotation, visit the Alliance of Genome Resources.


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Spondyloepimetaphyseal Dysplasia, Krakow Type term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Sik3 SIK family kinase 3 ISO OMIM NCBI chrNW_004955412:18,177,175...18,280,687
Ensembl chrNW_004955412:18,177,175...18,280,748
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11815
    Developmental Diseases 8416
      bone development disease 1258
        osteochondrodysplasia 413
          spondyloepimetaphyseal dysplasia 69
            Spondyloepimetaphyseal Dysplasia, Krakow Type 1
Path 2
Term Annotations click to browse term
  disease 11815
    disease of anatomical entity 11368
      musculoskeletal system disease 4925
        connective tissue disease 3405
          bone disease 2924
            bone development disease 1258
              osteochondrodysplasia 413
                spondyloepimetaphyseal dysplasia 69
                  Spondyloepimetaphyseal Dysplasia, Krakow Type 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.