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ONTOLOGY REPORT - ANNOTATIONS


Term:orofacial cleft 7
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Accession:DOID:0080400 term browser browse the term
Definition:An orofacial cleft that has_material_basis_in by homozygous mutation in the PVRL1 gene on chromosome 11q23. (DO)
Synonyms:primary_id: MESH:C563464
 alt_id: DOID:9002828;   RDO:0012712
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orofacial cleft 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NECTIN1 nectin cell adhesion molecule 1 JBrowse link 5 14,228,197 14,292,825 RGD:9068941
cleft lip-palate-ectodermal dysplasia syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NECTIN1 nectin cell adhesion molecule 1 JBrowse link 5 14,228,197 14,292,825 RGD:7240710
RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12008
    syndrome 4657
      ectodermal dysplasia 243
        orofacial cleft 7 1
          cleft lip-palate-ectodermal dysplasia syndrome 1
Path 2
Term Annotations click to browse term
  disease 12008
    Developmental Diseases 8250
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7060
        Congenital Abnormalities 3483
          Musculoskeletal Abnormalities 1275
            Craniofacial Abnormalities 1030
              Maxillofacial Abnormalities 203
                Jaw Abnormalities 201
                  orofacial cleft 112
                    orofacial cleft 7 1
                      cleft lip-palate-ectodermal dysplasia syndrome 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.