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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:Atelosteogenesis Type 3
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Accession:DOID:9004436 term browser browse the term
Synonyms:exact_synonym: AO3;   AOIII;   Atelosteogenesis Type III
 broad_synonym: FLNB-related spectrum disorder
 primary_id: MESH:C579928
 alt_id: OMIM:108721

show annotations for term's descendants           Sort by:
Atelosteogenesis Type 3 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Flnb filamin B ISO CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Atelosteogenesis type III
PMID:9536098 PMID:14991055 PMID:17576681 PMID:20301736 PMID:25741868 More... NCBI chr15:16,961,999...17,095,059
Ensembl chr15:16,962,003...17,095,006
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21089
    disease of anatomical entity 18156
      endocrine system disease 6707
        Dwarfism 874
          Atelosteogenesis Type 3 1
Path 2
Term Annotations click to browse term
  disease 21089
    disease of anatomical entity 18156
      musculoskeletal system disease 8196
        connective tissue disease 5725
          bone disease 4227
            bone development disease 2299
              osteochondrodysplasia 840
                atelosteogenesis 2
                  Atelosteogenesis Type 3 1
paths to the root