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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:Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies
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Accession:DOID:9004675 term browser browse the term
Synonyms:xref: OMIM:PS617877

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show annotations for term's descendants           Sort by:
Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Bmp2 bone morphogenetic protein 2 ISO ClinVar Annotator: match by term: Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies ClinVar PMID:25741868 PMID:28492532 PMID:29198724 NCBI chrNW_004936485:12,428,765...12,439,570
Ensembl chrNW_004936485:12,428,710...12,439,454 		JBrowse link
Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies 1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Bmp2 bone morphogenetic protein 2 ISO ClinVar Annotator: match by term: Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1 OMIM
ClinVar		 PMID:21671386 PMID:25741868 PMID:28492532 PMID:29198724 PMID:35227291 NCBI chrNW_004936485:12,428,765...12,439,570
Ensembl chrNW_004936485:12,428,710...12,439,454 		JBrowse link
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Scube3 signal peptide, CUB domain and EGF like domain containing 3 ISO ClinVar Annotator: match by term: Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 OMIM
ClinVar		 PMID:25741868 PMID:33308444 NCBI chrNW_004936476:23,962,956...23,987,629
Ensembl chrNW_004936476:23,966,847...23,998,663 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16465
    Developmental Disease 16381
      bone development disease 2182
        Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies 2
          Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies 1 1
          short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 1
Path 2
Term Annotations click to browse term
  disease 16465
    disease of anatomical entity 14117
      musculoskeletal system disease 7378
        connective tissue disease 5008
          bone disease 3672
            bone development disease 2182
              Dwarfism 810
                Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies 2
                  Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies 1 1
                  short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 1
paths to the root