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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:osteogenesis imperfecta type 6
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Accession:DOID:0110350 term browser browse the term
Definition:An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINF1 gene on chromosome 17p13.3. (DO)
Synonyms:exact_synonym: OI, type VI;   OI6;   osteogenesis imperfecta, type VI
 primary_id: MESH:C536047;   MESH:C567041
 alt_id: OMIM:613982
 xref: GARD:8700
For additional species annotation, visit the Alliance of Genome Resources.

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osteogenesis imperfecta type 6 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Serpinf1 serpin family F member 1 ISO OMIM NCBI chrNW_004955481:1,414,930...1,426,436
Ensembl chrNW_004955481:1,414,930...1,426,241
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11815
    Developmental Diseases 8416
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7381
        genetic disease 6958
          monogenic disease 5157
            osteogenesis imperfecta type 6 1
Path 2
Term Annotations click to browse term
  disease 11815
    disease of anatomical entity 11368
      Skin and Connective Tissue Diseases 4544
        connective tissue disease 3405
          bone disease 2924
            bone development disease 1258
              osteochondrodysplasia 413
                osteogenesis imperfecta 36
                  osteogenesis imperfecta type 6 1
paths to the root


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