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Term:orofacial cleft 5
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Accession:DOID:0080399 term browser browse the term
Definition:An orofacial cleft that has_material_basis_in mutation in the MSX1 gene on chromosome 4p16. (DO)
Synonyms:exact_synonym: OFC5;   nonsyndromic cleft lip with or without cleft palate 5
 primary_id: MESH:C563843
 alt_id: DOID:9001131;   OMIM:608874;   RDO:0012997
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orofacial cleft 5 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Msx1 msh homeobox 1 JBrowse link 14 77,712,262 77,716,061 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15036
    physical disorder 731
      orofacial cleft 110
        orofacial cleft 5 1
Path 2
Term Annotations click to browse term
  disease 15036
    Developmental Diseases 7870
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7198
        Congenital Abnormalities 3302
          Musculoskeletal Abnormalities 1196
            Craniofacial Abnormalities 956
              Maxillofacial Abnormalities 202
                Jaw Abnormalities 199
                  orofacial cleft 110
                    orofacial cleft 5 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.