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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:Omodysplasia 2
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Accession:DOID:9001743 term browser browse the term
Synonyms:exact_synonym: OMOD2;   Omodysplasia, Autosomal Dominant
 primary_id: MESH:C567664
 alt_id: OMIM:164745;   RDO:0015675
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
Omodysplasia 2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Fzd2 frizzled class receptor 2 ISO ClinVar Annotator: match by term: Omodysplasia 2 ClinVar
PMID:25759469 NCBI chr10:90,550,147...90,552,057
Ensembl chr10:90,550,147...90,552,057
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16023
    Pathological Conditions, Signs and Symptoms 8754
      Pathologic Processes 6130
        Disease Attributes 582
          Facies 260
            Omodysplasia 2 1
Path 2
Term Annotations click to browse term
  disease 16023
    disease of anatomical entity 15278
      Skin and Connective Tissue Diseases 5476
        connective tissue disease 4103
          bone disease 3534
            bone development disease 1343
              osteochondrodysplasia 446
                omodysplasia 2
                  Omodysplasia 2 1
paths to the root


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