ONTOLOGY REPORT - ANNOTATIONS


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
RGD:8554872

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Path 1
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  disease 14926
    physical disorder 748
      orofacial cleft 110
        orofacial cleft 5 1
Path 2
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  disease 14926
    Developmental Diseases 7782
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7103
        Congenital Abnormalities 3207
          Musculoskeletal Abnormalities 1198
            Craniofacial Abnormalities 953
              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.