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ONTOLOGY REPORT - ANNOTATIONS


Term:Meier-Gorlin syndrome 4
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Accession:DOID:0080515 term browser browse the term
Definition:A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDT1 gene on chromosome 16q24. (DO)
Synonyms:exact_synonym: MGORS4
 primary_id: OMIM:613804
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Meier-Gorlin syndrome 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cdt1 chromatin licensing and DNA replication factor 1 JBrowse link 19 55,381,565 55,386,511 RGD:8554872
RGD:7240710

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Path 1
Term Annotations click to browse term
  disease 15619
    syndrome 5154
      Meier-Gorlin syndrome 10
        Meier-Gorlin syndrome 4 1
Path 2
Term Annotations click to browse term
  disease 15619
    Developmental Diseases 8737
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7519
        Congenital Abnormalities 3592
          Musculoskeletal Abnormalities 1302
            Craniofacial Abnormalities 1046
              Maxillofacial Abnormalities 207
                Jaw Abnormalities 204
                  Micrognathism 38
                    Meier-Gorlin syndrome 10
                      Meier-Gorlin syndrome 4 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.