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RGD uses the Human Disease Ontology (DO, 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:sclerosteosis 1
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Accession:DOID:0060756 term browser browse the term
Definition:A sclerosteosis that has_material_basis_in homozygous mutation in the SOST gene on chromosome 17q21. (DO)
Synonyms:exact_synonym: SOST1
 primary_id: OMIM:269500
 alt_id: RDO:9003156
 xref: ICD10CM:M85.2
For additional species annotation, visit the Alliance of Genome Resources.

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sclerosteosis 1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Sost sclerostin ISO ClinVar Annotator: match by term: Sclerosteosis 1 OMIM
PMID:11179006 PMID:11181578 PMID:19072561 PMID:28492532 NCBI chr10:86,912,517...86,915,561
Ensembl chr10:86,911,517...86,915,561
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18162
    syndrome 9705
      chromosomal duplication syndrome 1047
        syndactyly 73
          sclerosteosis 2
            sclerosteosis 1 1
Path 2
Term Annotations click to browse term
  disease 18162
    disease of anatomical entity 17537
      musculoskeletal system disease 7230
        connective tissue disease 5013
          bone disease 3683
            bone development disease 1873
              dysostosis 439
                synostosis 287
                  syndactyly 73
                    sclerosteosis 2
                      sclerosteosis 1 1
paths to the root