ONTOLOGY REPORT - ANNOTATIONS


Term:Verheij Syndrome
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Accession:DOID:9003952 term browser browse the term
Synonyms:exact_synonym: CHROMOSOME 8q24.3 DELETION SYNDROME;   VRJS
 primary_id: OMIM:615583;   RDO:9001005
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Verheij Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Puf60 poly-U binding splicing factor 60 JBrowse link 7 117,129,237 117,140,234 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
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  disease 14875
    syndrome 4220
      Verheij Syndrome 1
Path 2
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  disease 14875
    Developmental Diseases 7711
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6750
        Congenital Abnormalities 3150
          Musculoskeletal Abnormalities 1191
            Craniofacial Abnormalities 949
              Verheij Syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.