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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:spondylometaepiphyseal dysplasia, short limb-hand type
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Accession:DOID:0112196 term browser browse the term
Definition:A spondyloepimetaphyseal dysplasia characterized by short stature, short limbs and hands, and typical radiological features which include platyspondyly, metaphyseal, and epiphyseal involvement, short tubular bones of the limbs, and abnormal calcification of cartilage that has_material_basis_in homozygous or compound heterozygous mutation in the DDR2 gene on chromosome 1q23.3. (DO)
Synonyms:exact_synonym: SMED Type II;   SMED type 2;   SMED, Short Limb-Abnormal Calcification Type;   SMED, Short Limb-Hand Type;   SMED-SL;   SMED-SL/AC;   spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome;   spondylometaepiphyseal dysplasia, short limb-abnormal calcification type
 primary_id: MESH:C564794
 alt_id: OMIM:271665
 xref: GARD:10616;   ORDO:93358


show annotations for term's descendants           Sort by:
spondylometaepiphyseal dysplasia, short limb-hand type term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ddr2 discoidin domain receptor tyrosine kinase 2 ISO CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome		 OMIM
CTD
ClinVar		 PMID:8434618 PMID:8818447 PMID:11375938 PMID:19110212 PMID:20223752 More... NCBI chr13:82,193,623...82,318,229
Ensembl chr13:82,195,463...82,317,363 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18969
    disease of anatomical entity 18249
      endocrine system disease 6821
        Dwarfism 865
          spondylometaepiphyseal dysplasia, short limb-hand type 1
Path 2
Term Annotations click to browse term
  disease 18969
    disease of anatomical entity 18249
      musculoskeletal system disease 8306
        connective tissue disease 5787
          bone disease 4302
            bone development disease 2307
              osteochondrodysplasia 861
                spondyloepimetaphyseal dysplasia 88
                  spondylometaepiphyseal dysplasia, short limb-hand type 1
paths to the root