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ONTOLOGY REPORT - ANNOTATIONS


Term:SWEENEY-COX SYNDROME
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Accession:DOID:9004224 term browser browse the term
Definition:A disease characterized by striking facial dysostosis, including hypertelorism, deficiencies of the eyelids and facial bones, cleft palate/velopharyngeal insufficiency, and low-set cupped ears. (OMIM)
Synonyms:exact_synonym: SWCOS
 primary_id: OMIM:617746;   RDO:9005206
For additional species annotation, visit the Alliance of Genome Resources.


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SWEENEY-COX SYNDROME term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Twist1 twist family bHLH transcription factor 1 JBrowse link 6 53,401,241 53,403,235 RGD:8554872
RGD:7240710

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Path 1
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  disease 14759
    syndrome 4210
      SWEENEY-COX SYNDROME 1
Path 2
Term Annotations click to browse term
  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        Congenital Abnormalities 3137
          Musculoskeletal Abnormalities 1185
            Craniofacial Abnormalities 945
              SWEENEY-COX SYNDROME 1
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