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Term:orofacial cleft 10
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Accession:DOID:0080403 term browser browse the term
Definition:An orofacial cleft that has_material_basis_in mutation in the SUMO1 gene on chromosome 2q33. (DO)
Synonyms:exact_synonym: OFC10;   nonsyndromic cleft lip with or without cleft palate 10
 primary_id: MESH:C566605
 alt_id: DOID:9006702;   OMIM:613705;   RDO:0014918
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orofacial cleft 10 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Irf6 interferon regulatory factor 6 JBrowse link 13 111,870,121 111,889,328 RGD:8554872
G Sumo1 small ubiquitin-like modifier 1 JBrowse link 9 66,453,428 66,483,614 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15599
    physical disorder 738
      orofacial cleft 114
        orofacial cleft 10 2
Path 2
Term Annotations click to browse term
  disease 15599
    Developmental Diseases 8726
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7507
        Congenital Abnormalities 3579
          Musculoskeletal Abnormalities 1296
            Craniofacial Abnormalities 1040
              Maxillofacial Abnormalities 207
                Jaw Abnormalities 204
                  orofacial cleft 114
                    orofacial cleft 10 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.