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ONTOLOGY REPORT - ANNOTATIONS


Term:Singleton-Merten Syndrome 2
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Accession:DOID:9002133 term browser browse the term
Definition:A syndrome with variable expression of glaucoma, aortic calcification, and skeletal abnormalities, without dental anomalies. (OMIM)
Synonyms:exact_synonym: SGMRT2
 primary_id: OMIM:616298
 alt_id: RDO:9001557
For additional species annotation, visit the Alliance of Genome Resources.


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Singleton-Merten Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ddx58 DEXD/H-box helicase 58 JBrowse link 5 56,486,584 56,536,898 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    syndrome 4210
      Singleton Merten Syndrome 2
        Singleton-Merten Syndrome 2 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        sensory system disease 4231
          mouth disease 655
            tooth disease 221
              teeth hard tissue disease 36
                dental enamel hypoplasia 30
                  Singleton Merten Syndrome 2
                    Singleton-Merten Syndrome 2 1
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